rs17110747

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs17110747(A;A)

Make rs17110747(A;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

72032174

Gene

TPH2

is a	snp
is	mentioned by
dbSNP	rs17110747
dbSNP (classic)	rs17110747
ClinGen	rs17110747
ebi	rs17110747
HLI	rs17110747
Exac	rs17110747
Gnomad	rs17110747
Varsome	rs17110747
LitVar	rs17110747
Map	rs17110747
PheGenI	rs17110747
Biobank	rs17110747
1000 genomes	rs17110747
hgdp	rs17110747
ensembl	rs17110747
geneview	rs17110747
scholar	rs17110747
google	rs17110747
pharmgkb	rs17110747
gwascentral	rs17110747
openSNP	rs17110747
23andMe	rs17110747
SNPshot	rs17110747
SNPdbe	rs17110747
MSV3d	rs17110747
GWAS Ctlg	rs17110747

GMAF

0.1529

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

[PMID 21396719] Influence of TPH2 variants on diagnosis and response to treatment in patients with major depression, bipolar disorder and schizophrenia

[PMID 19272410] Tryptophan hydroxylase 2 gene is associated with major depression and antidepressant treatment response.

ClinVar
Risk	rs17110747(A;A)
Alt	rs17110747(A;A)
Reference	Rs17110747(G;G)
Significance	Probable-non-pathogenic
Disease	Tryptophan 5-monooxygenase deficiency
Variation	info
Gene	TPH2
CLNDBN	Tryptophan 5-monooxygenase deficiency
Reversed	0
HGVS	NC_000012.11:g.72425954G>A
CLNSRC
CLNACC	RCV000263324.1,