rs1800443

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	3.5	Rare DRD4 polymorphism
(G;T)	3	Uncommon DRD4 polymorphism
(T;T)	0	common in clinvar

Reference

GRCh37 37.1/131

Chromosome

11

Position

639830

Gene

DRD4

is a	snp
is	mentioned by
dbSNP	rs1800443
dbSNP (classic)	rs1800443
ClinGen	rs1800443
ebi	rs1800443
HLI	rs1800443
Exac	rs1800443
Gnomad	rs1800443
Varsome	rs1800443
LitVar	rs1800443
Map	rs1800443
PheGenI	rs1800443
Biobank	rs1800443
1000 genomes	rs1800443
hgdp	rs1800443
ensembl	rs1800443
geneview	rs1800443
scholar	rs1800443
google	rs1800443
pharmgkb	rs1800443
gwascentral	rs1800443
openSNP	rs1800443
23andMe	rs1800443
SNPshot	rs1800443
SNPdbe	rs1800443
MSV3d	rs1800443
GWAS Ctlg	rs1800443

GMAF

0.01194

Max Magnitude

3.5

?	(G;G) (G;T) (T;T)	28

OMIM	126452
Desc	DOPAMINE RECEPTOR D4 POLYMORPHISM
Variant	0002
Related	also

ClinVar
Risk	Rs1800443(G;G)
Alt	Rs1800443(G;G)
Reference	Rs1800443(T;T)
Significance	Non-pathogenic
Disease	DOPAMINE RECEPTOR D4 POLYMORPHISM
Variation	info
Gene	DRD4
CLNDBN	DOPAMINE RECEPTOR D4 POLYMORPHISM
Reversed	0
HGVS	NC_000011.9:g.639830T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018255.3,

[PMID 19584173] Kininogen gene (KNG) variation has a consistent effect on aldosterone response to antihypertensive drug therapy: the GERA study.