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rs1800443

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 3.5 Rare DRD4 polymorphism
(G;T) 3 Uncommon DRD4 polymorphism
(T;T) 0 common in clinvar
ReferenceGRCh37 37.1/131
Chromosome11
Position639830
GeneDRD4
is asnp
is mentioned by
dbSNPrs1800443
ebirs1800443
HLIrs1800443
Exacrs1800443
Varsomers1800443
Maprs1800443
PheGenIrs1800443
hapmaprs1800443
1000 genomesrs1800443
hgdprs1800443
ensemblrs1800443
gopubmedrs1800443
geneviewrs1800443
scholarrs1800443
googlers1800443
pharmgkbrs1800443
gwascentralrs1800443
openSNPrs1800443
23andMers1800443
23andMe allrs1800443
SNP Nexus

SNPshotrs1800443
SNPdbers1800443
MSV3drs1800443
GWAS Ctlgrs1800443
GMAF0.01194
Max Magnitude3.5
? (G;G) (G;T) (T;T) 28
OMIM126452
DescDOPAMINE RECEPTOR D4 POLYMORPHISM
Variant0002
Relatedalso


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 RCV000018255.2,



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