rs1800496

Orientation

minus

Stabilized

minus

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

Make rs1800496(C;T)

Make rs1800496(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

113412766

Gene

DRD2

is a	snp
is	mentioned by
dbSNP	rs1800496
dbSNP (classic)	rs1800496
ClinGen	rs1800496
ebi	rs1800496
HLI	rs1800496
Exac	rs1800496
Gnomad	rs1800496
Varsome	rs1800496
LitVar	rs1800496
Map	rs1800496
PheGenI	rs1800496
Biobank	rs1800496
1000 genomes	rs1800496
hgdp	rs1800496
ensembl	rs1800496
geneview	rs1800496
scholar	rs1800496
google	rs1800496
pharmgkb	rs1800496
gwascentral	rs1800496
openSNP	rs1800496
23andMe	rs1800496
SNPshot	rs1800496
SNPdbe	rs1800496
MSV3d	rs1800496
GWAS Ctlg	rs1800496

GMAF

0.001377

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

origins associated with an independent aspect of decision making in a learning paradigm

[PMID 19512960] Genetic diagnostics of functional variants of the human dopamine D2 receptor gene

[PMID 18332877] Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan.

ClinVar
Risk	rs1800496(T;T)
Alt	rs1800496(T;T)
Reference	Rs1800496(C;C)
Significance	Other
Disease	not specified Dystonia
Variation	info
Gene	DRD2
CLNDBN	not specified Dystonia
Reversed	1
HGVS	NC_000011.9:g.113283488G>A
CLNSRC
CLNACC	RCV000246273.2, RCV000458798.1,