Serotonin/all

Serotonin synthesis[edit]

TPH1

	On chromosome	Chromosome position	In gene	Summary
rs366590	11	16,850,893	PLEKHA7
rs2108977	11	18,019,049	TPH1
rs7933505	11	18,024,440	TPH1
rs1799913	11	18,025,708	TPH1	heroin addiction in hispanics
rs1799913(C;C)	11	18,025,708	TPH1	Hispanics may be at increased risk of heroin addiction.
rs1800532	11	18,026,269	TPH1
rs211105	11	18,033,757	TPH1
rs684302	11	18,038,806	TPH1
rs623580	11	18,042,430	TPH1

TPH2

	On chromosome	Chromosome position	In gene	Summary
rs4489789	12	70,665,152	PTPRR
rs4489789(T;T)	12	70,665,152	PTPRR	common in complete genomics
rs2175711	12	70,679,733	PTPRR
rs2203231	12	70,686,988	PTPRR
rs4570625(G;G)	12	71,938,143	TPH2	maybe: higher scores on anxiety-related personality traits; greater placebo response
rs4570625(G;T)	12	71,938,143	TPH2	normal
rs4570625(T;T)	12	71,938,143	TPH2	normal
rs4570625	12	71,938,143	TPH2
rs11178997(T;T)	12	71,938,373	TPH2
rs11178997	12	71,938,373	TPH2
rs11178998(A;A)	12	71,938,935	TPH2	common in clinvar
rs11178998	12	71,938,935	TPH2
rs4341581	12	71,941,293	TPH2
rs78162420	12	71,941,600	TPH2
rs78162420(C;C)	12	71,941,600	TPH2	common in clinvar
rs7954758	12	71,942,014	TPH2
rs10748185	12	71,942,075	TPH2
rs4565946(C;C)	12	71,942,989	TPH2	Risk of early-onset OCD
rs4565946(T;T)	12	71,942,989	TPH2	None
rs4565946(C;T)	12	71,942,989	TPH2
rs4565946	12	71,942,989	TPH2
rs11179000	12	71,944,848	TPH2
rs11179002	12	71,948,504	TPH2
rs1843809(T;T)	12	71,954,918	TPH2	Most common genotype worldwide
rs1843809(G;G)	12	71,954,918	TPH2	slightly decreased risk for ADHD
rs1843809	12	71,954,918	TPH2
rs7955501	12	71,956,246	TPH2
rs1386496	12	71,957,010	TPH2
rs1386494	12	71,958,763	TPH2
rs1386494(T;C)	12	71,958,763	TPH2
rs1386493	12	71,961,399	TPH2
rs2171363	12	71,966,484	TPH2
rs7963720	12	71,972,406	TPH2
rs17110563	12	71,972,526	TPH2
rs17110563(C;C)	12	71,972,526	TPH2	common in complete genomics
rs4760816	12	71,978,821	TPH2
rs120074176	12	71,979,053	TPH2
rs120074176(C;T)	12	71,979,053	TPH2	Possible increased risk for ADHD and other psychiatric disorders
rs120074176(C;C)	12	71,979,053	TPH2	common in complete genomics
rs7305115(A;G)	12	71,979,082	TPH2	risk of suicide behavior
rs7305115(G;G)	12	71,979,082	TPH2	risk of suicide behavior
rs7305115(A;A)	12	71,979,082	TPH2	Individuals showed a significantly lower risk of suicide behavior than those with the A/G or G/G genotype
rs7305115	12	71,979,082	TPH2
rs11179027	12	71,983,532	TPH2
rs10506645	12	71,991,720	TPH2
rs1007023	12	71,994,594	TPH2
rs1386497	12	71,998,510	TPH2
rs4760820	12	72,003,216	TPH2
rs1386498	12	72,004,363	TPH2
rs1487278	12	72,007,071	TPH2
... further results

DDC

	On chromosome	Chromosome position	In gene	Summary
rs2060762	7	50,461,686	DDC
rs2242041	7	50,461,751	DDC
rs771317809(C;C)	7	50,470,140	DDC	common in clinvar
rs771317809	7	50,470,140	DDC
rs3757472	7	50,470,285	DDC
rs11761683	7	50,475,181	DDC
rs11761683(T;T)	7	50,475,181	DDC	Migraine
rs201951824	7	50,476,625	DDC
rs201951824(C;C)	7	50,476,625	DDC	common in clinvar
rs11575461	7	50,479,485	DDC
rs12718541(A;A)	7	50,482,446	DDC	Nicotine dependence
rs12718541	7	50,482,446	DDC
rs1451371	7	50,485,353	DDC
rs137853209(T;T)	7	50,495,369	DDC	common in clinvar
rs137853209	7	50,495,369	DDC
rs137853212(G;G)	7	50,499,201	DDC	common in clinvar
rs137853212	7	50,499,201	DDC
rs3779084	7	50,501,037	DDC
rs880028	7	50,502,438	DDC
rs137853208(C;C)	7	50,504,025	DDC	common in clinvar
rs137853208	7	50,504,025	DDC
rs6592961	7	50,505,192	DDC
rs7809758	7	50,505,635	DDC
rs1470750	7	50,508,950	DDC
rs3735273	7	50,529,166	DDC
rs137853210	7	50,529,339	DDC
rs137853210(A;A)	7	50,529,339	DDC	common in clinvar
rs998850	7	50,539,690	DDC DDC-AS1
rs137853207	7	50,539,926	DDC DDC-AS1
rs137853207(G;G)	7	50,539,926	DDC DDC-AS1	common in clinvar
rs137853211	7	50,539,958	DDC DDC-AS1
rs137853211(C;C)	7	50,539,958	DDC DDC-AS1	common in clinvar
rs7809234	7	50,542,681	DDC DDC-AS1
rs1085307991	7	50,544,015	DDC
rs1085307991(T;T)	7	50,544,015	DDC	common in clinvar
rs6264(G;G)	7	50,544,037	DDC	common in complete genomics
rs6264	7	50,544,037	DDC
rs2044859(T;T)	7	50,544,864	DDC	Migraine
rs2044859	7	50,544,864	DDC
rs11974297(G;G)	7	50,550,562	DDC	Migraine
rs11974297	7	50,550,562	DDC
rs2329340	7	50,552,531	DDC
rs2329340(T;T)	7	50,552,531	DDC	M
rs1451375	7	50,555,014	DDC
rs921451	7	50,555,587	DDC
rs3837091(AGAG;AGAG)	7	50,561,043	DDC	common in clinvar
rs3837091	7	50,561,043	DDC
rs12540874	7	50,597,225	GRB10

Serotonin degradation[edit]

MAOA

	On chromosome	Chromosome position	In gene	Summary
rs5953210	X	43,654,798	MAOA
rs3788862	X	43,658,116	MAOA
rs5906883	X	43,667,695	MAOA
rs1465107	X	43,678,769	MAOA
rs796065312	X	43,683,572	MAOA
rs796065312(C;C)	X	43,683,572	MAOA	common in clinvar
rs5906957	X	43,688,062	MAOA
rs909525	X	43,693,955	MAOA	Best proxy for Warrior Gene repeats.
rs909525(A;A)	X	43,693,955	MAOA	Probably MAOA 4 or 5 repeats: not Warrior Gene.
rs909525(G;G)	X	43,693,955	MAOA	Perhaps MAOA 3 repeats: Warrior Gene?
rs909525(A;G)	X	43,693,955	MAOA	Probably one Warrior Gene and one non-Warrior Gene.
rs2283725	X	43,700,729	MAOA
rs796065311	X	43,731,344	MAOA
rs796065311(-;-)	X	43,731,344	MAOA	common in clinvar
rs587777457	X	43,731,695	MAOA
rs587777457(G;G)	X	43,731,695	MAOA	common in clinvar
rs72554632(C;C)	X	43,731,784	MAOA	common in clinvar
rs72554632(T;T)	X	43,731,784	MAOA	possible mental retardation
rs72554632(C;T)	X	43,731,784	MAOA	Carrier for Brunner's Syndrome
rs72554632	X	43,731,784	MAOA
rs6323(G;G)	X	43,731,789	MAOA	Increased monoamine oxidase A activity
rs6323(T;T)	X	43,731,789	MAOA	reduced MAOA activity
rs6323	X	43,731,789	MAOA	Monoamine oxidase A activity
rs3027400	X	43,733,516	MAOA
rs2235186	X	43,736,181	MAOA
rs2072743	X	43,740,274	MAOA
rs979606	X	43,741,895	MAOA
rs1137070	X	43,744,144	MAOA
rs3027407	X	43,745,594	MAOA
rs3027409	X	43,747,786	MAOA
rs3027409(T;T)	X	43,747,786	MAOA	common on affy axiom data
rs6609257	X	43,753,461	MAOA

Serotonin transporters[edit]

SLC6A4/SERT

	On chromosome	Chromosome position	In gene	Summary
rs3813034(A;A)	17	30,197,786	SLC6A4	common in clinvar
rs3813034	17	30,197,786	SLC6A4
rs1042173	17	30,197,993	SLC6A4
rs1042173(G;G)	17	30,197,993	SLC6A4	normal
rs1042173(G;T)	17	30,197,993	SLC6A4	normal
rs1042173(T;T)	17	30,197,993	SLC6A4	among alcoholics, likely to be heavier drinkers
rs12449783	17	30,200,635	SLC6A4
rs3794808	17	30,204,775	SLC6A4
rs2054847	17	30,204,995	SLC6A4
rs34388196	17	30,207,451	SLC6A4
rs28914832(A;A)	17	30,211,356	SLC6A4	common in complete genomics
rs28914832	17	30,211,356	SLC6A4
rs140701(G;G)	17	30,211,514	SLC6A4	Normal risk for anxiety disorders
rs140701	17	30,211,514	SLC6A4
rs140701(A;A)	17	30,211,514	SLC6A4	Increased risk for anxiety disorders
rs140701(A;G)	17	30,211,514	SLC6A4	Increased risk for anxiety disorders
rs4583306	17	30,211,697	SLC6A4
rs140700	17	30,216,371	SLC6A4
rs140700(C;C)	17	30,216,371	SLC6A4
rs2020942	17	30,219,896	SLC6A4
rs2020942(A;G)	17	30,219,896	SLC6A4	common in complete genomics
rs8076005	17	30,220,192	SLC6A4
rs11080122	17	30,220,317	SLC6A4
rs57098334	17	30,221,570	SLC6A4
rs6354	17	30,222,880	SLC6A4
rs6354(C;C)	17	30,222,880	SLC6A4	common in clinvar
rs25528	17	30,222,960	SLC6A4
rs2020936	17	30,223,796	SLC6A4
rs12150214	17	30,223,870	SLC6A4
rs2066713(C;T)	17	30,224,647	SLC6A4	common in complete genomics
rs2066713	17	30,224,647	SLC6A4
rs4251417(G;G)	17	30,224,840	SLC6A4
rs4251417	17	30,224,840	SLC6A4
rs8071667	17	30,225,755	SLC6A4
rs16965628	17	30,228,407	SLC6A4
rs2020934	17	30,234,442	SLC6A4
rs2020933	17	30,234,737	SLC6A4
rs2020933(T;T)	17	30,234,737	SLC6A4
rs25533	17	30,235,874	SLC6A4 LOC105371720
rs25533(T;T)	17	30,235,874	SLC6A4 LOC105371720	common in complete genomics
rs956304	17	30,236,544	SLC6A4 LOC105371720
rs25532(C;C)	17	30,237,152	SLC6A4 LOC105371720	may be part of a haplotype associated with OCD
rs25532	17	30,237,152	SLC6A4 LOC105371720
rs25532(C;T)	17	30,237,152	SLC6A4 LOC105371720	may be part of a haplotype associated with OCD
rs25532(T;T)	17	30,237,152	SLC6A4 LOC105371720	normal
rs4795541(-;-)	17	30,237,299	SLC6A4 LOC105371720	normal
rs4795541(-;AGATGCTGGGGGGGCTGCAGGGGGGATGCTGGGGGTGCAGGGG)	17	30,237,299	SLC6A4 LOC105371720	complex; see details
rs4795541(AGATGCTGGGGGGGCTGCAGGGGGGATGCTGGGGGTGCAGGGG;AGATGCTGGGGGGGCTGCAGGGGGGATGCTGGGGGTGCAGGGG)	17	30,237,299	SLC6A4 LOC105371720	complex; see details
rs4795541	17	30,237,299	SLC6A4 LOC105371720
rs25531	17	30,237,328	SLC6A4 LOC105371720
... further results

SLC18A2/VMAT2

	On chromosome	Chromosome position	In gene	Summary
rs60912143	10	117,241,017	SLC18A2 LOC105378500
rs363387	10	117,244,053	SLC18A2 LOC105378500
rs363387(T;T)	10	117,244,053	SLC18A2 LOC105378500
rs1060499741(C;C)	10	117,255,281	SLC18A2	common in clinvar
rs1060499741	10	117,255,281	SLC18A2
rs2015586	10	117,262,226	SLC18A2
rs363224(A;A)	10	117,263,062	SLC18A2	Protective against TD occurrence
rs363224	10	117,263,062	SLC18A2
rs363227	10	117,267,055	SLC18A2
rs363276	10	117,274,298	SLC18A2

Serotonin receptors[edit]

HTR1A

	On chromosome	Chromosome position	In gene	Summary
rs7445832	5	63,290,474
rs878567	5	63,960,164	HTR1A
rs6449693	5	63,960,191	HTR1A
rs1800044	5	63,961,061	HTR1A
rs1800044(G;G)	5	63,961,061	HTR1A	common/normal
rs34118353	5	63,961,168	HTR1A
rs112846276	5	63,961,175	HTR1A
rs6294	5	63,961,426	HTR1A
rs367956927	5	63,962,199	HTR1A
rs367956927(D;D)	5	63,962,199	HTR1A	Miscall by Ancestry
rs367956927(T;T)	5	63,962,199	HTR1A	common in clinvar
rs6295(G;G)	5	63,962,738	HTR1A	common in clinvar
rs6295	5	63,962,738	HTR1A
rs113195492	5	63,962,787	HTR1A

HTR1B

	On chromosome	Chromosome position	In gene
rs13212041	6	77,461,407	HTR1B LOC105377864
rs13212041(C;C)	6	77,461,407	HTR1B LOC105377864
rs6296	6	77,462,543	HTR1B LOC105377864
rs770106646	6	77,462,742	HTR1B LOC105377864
rs130058	6	77,463,564	HTR1B LOC105377864
rs11568817	6	77,463,665	HTR1B LOC105377864
rs4140535	6	77,465,335	HTR1B LOC105377864

HTR1D

HTR1E

	On chromosome	Chromosome position	In gene	Summary
rs3828741	6	87,015,956	HTR1E
rs3828741(C;C)	6	87,015,956	HTR1E	common in complete genomics
rs6303	6	87,016,119	HTR1E

HTR1F

HTR2A

	On chromosome	Chromosome position	In gene	Summary
rs3125	13	46,834,716	HTR2A
rs6314(T;T)	13	46,834,899	HTR2A	average
rs6314	13	46,834,899	HTR2A
rs6314(C;C)	13	46,834,899	HTR2A	higher risk for RA
rs6314(C;T)	13	46,834,899	HTR2A	higher risk for RA; better response to paroxetine as treatment for depression
rs7322347	13	46,835,968	HTR2A
rs7997012(A;A)	13	46,837,850	HTR2A	~18% more likely to respond to citalopram
rs7997012(G;G)	13	46,837,850	HTR2A	~18% less likely to respond to citalopram
rs7997012	13	46,837,850	HTR2A
rs7997012(A;G)	13	46,837,850	HTR2A	normal risk
rs3742278	13	46,845,442	HTR2A
rs6561333	13	46,846,177	HTR2A
rs1923886	13	46,849,156	HTR2A
rs7330461	13	46,849,430	HTR2A
rs1745837	13	46,850,677	HTR2A HTR2A-AS1
rs655888	13	46,854,046	HTR2A HTR2A-AS1
rs2296972	13	46,854,336	HTR2A HTR2A-AS1
rs643627(T;C)	13	46,854,476	HTR2A HTR2A-AS1
rs643627	13	46,854,476	HTR2A HTR2A-AS1
rs7984966	13	46,855,311	HTR2A HTR2A-AS1
rs2224721	13	46,858,019	HTR2A
rs2224721(C;C)	13	46,858,019	HTR2A	common/normal
rs9316233	13	46,859,220	HTR2A
rs2770292	13	46,860,971	HTR2A
rs659734	13	46,861,148	HTR2A
rs659734(T;T)	13	46,861,148	HTR2A	common in complete genomics
rs1928042	13	46,863,081	HTR2A
rs2770296	13	46,866,425	HTR2A
rs1328674(A;G)	13	46,867,572	HTR2A	higher risk for RA
rs1328674(G;G)	13	46,867,572	HTR2A	average
rs1328674	13	46,867,572	HTR2A
rs1328674(A;A)	13	46,867,572	HTR2A	higher risk for RA
rs582385	13	46,871,859	HTR2A
rs1928040	13	46,873,101	HTR2A
rs2770304	13	46,881,230	HTR2A
rs927544	13	46,881,916	HTR2A
rs17288723	13	46,883,558	HTR2A
rs594242(C;G)	13	46,883,917	HTR2A
rs594242	13	46,883,917	HTR2A
rs9534505(G;G)	13	46,886,609	HTR2A	common in complete genomics
rs9534505	13	46,886,609	HTR2A
rs2070037	13	46,892,935	HTR2A
rs6313(T;T)	13	46,895,805	HTR2A	depression, panic, stress response
rs6313(C;C)	13	46,895,805	HTR2A	higher risk for RA
rs6313(C;T)	13	46,895,805	HTR2A	higher risk for RA
rs6313	13	46,895,805	HTR2A
rs6311	13	46,897,343	HTR2A
rs6311(T;T)	13	46,897,343	HTR2A	Normal (lower) risk of sexual dysfunction when taking SSRI Antidepressants.
rs6311(C;C)	13	46,897,343	HTR2A	3.6x increased risk of sexual dysfunction when taking SSRI Antidepressants.
rs6311(C;T)	13	46,897,343	HTR2A	Normal risk of sexual dysfunction when taking SSRI Antidepressants.

HTR2B

	On chromosome	Chromosome position	In gene	Summary
rs77982984	2	231,108,801	HTR2B PSMD1
rs17440378	2	231,114,641	HTR2B PSMD1
rs10194776	2	231,115,305	HTR2B PSMD1
rs16827801	2	231,116,063	HTR2B PSMD1
rs79874540	2	231,123,707	HTR2B PSMD1
rs79874540(C;C)	2	231,123,707	HTR2B PSMD1	common in complete genomics
rs79874540(T;T)	2	231,123,707	HTR2B PSMD1	Increased risk for impulsive/aggressive behaviour when drunk
rs79874540(C;T)	2	231,123,707	HTR2B PSMD1	2-3 fold higher risk of impulsive/aggressive behaviour when drunk

HTR2C

	On chromosome	Chromosome position	In gene	Summary
rs521018	X	114,583,441	HTR2C
rs498207	X	114,583,649	HTR2C
rs3813928	X	114,583,809	HTR2C
rs3813929(C;T)	X	114,584,047	HTR2C	normal
rs3813929(T;T)	X	114,584,047	HTR2C	normal
rs3813929	X	114,584,047	HTR2C
rs3813929(C;C)	X	114,584,047	HTR2C	possible weight gain if taking olanzapine
rs518147(G;G)	X	114,584,109	HTR2C	normal
rs518147(C;C)	X	114,584,109	HTR2C	less weight gain if taking olanzapine
rs518147	X	114,584,109	HTR2C
rs518147(C;G)	X	114,584,109	HTR2C	normal
rs498177	X	114,590,222	HTR2C
rs2192372	X	114,657,295	HTR2C
rs6318(C;C)	X	114,731,326	HTR2C LOC105373313	1.4x increased risk for cardiac events in patients; apparently stress (cortisol) related
rs6318(C;G)	X	114,731,326	HTR2C LOC105373313	Female only, since on X ch; appears to mostly be = to common (G;G) genotype
rs6318	X	114,731,326	HTR2C LOC105373313
rs6318(G;G)	X	114,731,326	HTR2C LOC105373313	common in clinvar
rs2428707	X	114,765,807	HTR2C LOC105373313
rs4272555	X	114,849,062	HTR2C
rs1414334	X	114,903,581	HTR2C
rs1414334(C;C)	X	114,903,581	HTR2C	associated with metabolic syndrome when taking antipsychotics

HTR3A

	On chromosome	Chromosome position	In gene	Summary
rs1150226	11	113,974,819	HTR3A
rs1150226(C;C)	11	113,974,819	HTR3A	common in complete genomics
rs1062613	11	113,975,284	HTR3A
rs33940208	11	113,975,355	HTR3A
rs1985242	11	113,977,551	HTR3A
rs2276302	11	113,979,418	HTR3A
rs10160548	11	113,985,959	HTR3A
rs1176713	11	113,989,703	HTR3A

HTR3B

	On chromosome	Chromosome position	In gene
rs10789970	11	113,903,224	HTR3B
rs3758987	11	113,904,553	HTR3B
rs45460698(AAG;AAG)	11	113,904,832	HTR3B
rs45460698	11	113,904,832	HTR3B
rs11606194(T;T)	11	113,910,259	HTR3B
rs11606194	11	113,910,259	HTR3B
rs4938056	11	113,915,817	HTR3B
rs1176746	11	113,931,879	HTR3B
rs1176744	11	113,932,306	HTR3B
rs2276305	11	113,932,382	HTR3B
rs2276307	11	113,933,165	HTR3B
rs2276307(A;A)	11	113,933,165	HTR3B
rs3782025	11	113,936,885	HTR3B
rs1672717	11	113,942,011	HTR3B
rs1185027	11	113,946,934	HTR3B

HTR3C

	On chromosome	Chromosome position	In gene	Summary
rs6766410	3	184,056,974	HTR3C
rs6807362(C;G)	3	184,060,222	HTR3C	normal autism risk
rs6807362	3	184,060,222	HTR3C
rs6807362(C;C)	3	184,060,222	HTR3C	increased autism risk
rs6807362(G;G)	3	184,060,222	HTR3C	decreased autism risk
rs6807670	3	184,060,510	HTR3C
rs398124646	3	185,254,016	EHHADH MIR5588
rs398124646(G;G)	3	185,254,016	EHHADH MIR5588	common in clinvar

HTR3D

	On chromosome	Chromosome position	In gene	Summary
rs6443930	3	184,036,506	HTR3D

HTR3E

	On chromosome	Chromosome position	In gene	Summary
rs7627615	3	184,100,628	HTR3E HTR3E-AS1
rs56109847(G;G)	3	184,106,769	HTR3E HTR3E-AS1	common in complete genomics
rs62625044	3	184,106,769	HTR3E
rs56109847	3	184,106,769	HTR3E HTR3E-AS1

HTR4

	On chromosome	Chromosome position	In gene	Summary
rs515726208(G;G)	5	147,824,702	SPINK1	common in clinvar
rs515726208	5	147,824,702	SPINK1
rs148954387	5	147,828,020	SPINK1
rs148954387(A;A)	5	147,828,020	SPINK1	common in clinvar
rs515726207(A;A)	5	147,828,056	SPINK1	common in clinvar
rs515726207	5	147,828,056	SPINK1
rs515726206(A;A)	5	147,828,066	SPINK1	common in clinvar
rs515726206	5	147,828,066	SPINK1
rs17107315(C;T)	5	147,828,115	SPINK1	risk of pancreatitis
rs17107315(A;A)	5	147,828,115	SPINK1	common genotype
rs17107315(C;C)	5	147,828,115	SPINK1	risk of pancreatitis
rs17107315	5	147,828,115	SPINK1
rs17107315(T;T)	5	147,828,115	SPINK1	normal
rs104893939	5	147,831,537	SPINK1
rs104893939(T;T)	5	147,831,537	SPINK1	common in clinvar
rs193922659(C;C)	5	147,831,551	SPINK1	common in clinvar
rs193922659	5	147,831,551	SPINK1
rs104893938	5	147,831,576	SPINK1
rs104893938(T;T)	5	147,831,576	SPINK1	common in clinvar
rs28935768	5	147,831,576	SPINK1
rs28935768(T;T)	5	147,831,576	SPINK1
rs142703147	5	147,835,718	SPINK1
rs891992	5	147,845,951
rs1432982	5	147,854,895	C5orf46
rs10035432	5	147,855,193	C5orf46
rs11168048	5	148,462,790	HTR4 LOC107986462
rs3995090	5	148,466,252	HTR4 LOC107986462
rs7733088	5	148,476,770	HTR4 LOC107986462
rs9325104	5	148,543,814	HTR4 LOC107986462

HTR5A

	On chromosome	Chromosome position	In gene	Summary
rs10239794(C;T)	7	154,508,809	DPP6	Probably benign; only one 2008 study reports 1.3x higher risk for ALS
rs10239794	7	154,508,809	DPP6
rs10239794(T;T)	7	154,508,809	DPP6	common/normal
rs10239794(C;C)	7	154,508,809	DPP6	Probably benign; one 2008 study reports 1.3x higher risk for ALS
rs1800883	7	155,070,881	HTR5A HTR5A-AS1
rs6320	7	155,070,911	HTR5A HTR5A-AS1

HTR6

	On chromosome	Chromosome position	In gene	Summary
rs1805054	1	19,666,020	HTR6
rs1805054(C;C)	1	19,666,020	HTR6	common in complete genomics
rs4654903	1	19,874,497	LOC105376823

HTR7

	On chromosome	Chromosome position	In gene	Summary
rs12249377	10	90,833,199	HTR7
rs1935349	10	90,834,586	HTR7
rs11187033	10	92,502,602	IDE
rs1832196	10	92,508,577	IDE
rs7895832(A;A)	10	92,516,769	IDE	common in complete genomics
rs7895832	10	92,516,769	IDE
rs7078413	10	92,530,727	IDE
rs11187061	10	92,545,652	IDE
rs17107734(C;C)	10	92,545,660	IDE	common in complete genomics
rs17107734	10	92,545,660	IDE
rs11187065	10	92,552,167	IDE
rs1999764	10	92,560,382	IDE
rs4646954	10	92,574,070	IDE
rs4646954(G;G)	10	92,574,070	IDE	common in complete genomics
rs4646953	10	92,574,198	IDE
rs3758505(T;T)	10	92,575,021	IDE	common in complete genomics
rs3758505	10	92,575,021	IDE
rs6583826	10	92,588,073
rs886041477(TGC;TGC)	10	92,593,399	KIF11	common in clinvar
rs886041477	10	92,593,399	KIF11
rs1057524736(G;G)	10	92,593,453	KIF11	common in clinvar
rs1057524736	10	92,593,453	KIF11
rs1064796738	10	92,606,655	KIF11
rs1064796738(C;C)	10	92,606,655	KIF11	common in clinvar
rs797045650	10	92,609,068	KIF11
rs797045650(A;A)	10	92,609,068	KIF11	common in clinvar

Serotonin/all

Contents

Serotonin synthesis[edit]

Serotonin degradation[edit]

Serotonin transporters[edit]

Serotonin receptors[edit]