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rs4937391

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs4937391(A;A)
Make rs4937391(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position128916399
GeneKCNJ5
is asnp
is mentioned by
dbSNPrs4937391
dbSNP (classic)rs4937391
ClinGenrs4937391
ebirs4937391
HLIrs4937391
Exacrs4937391
Gnomadrs4937391
Varsomers4937391
LitVarrs4937391
Maprs4937391
PheGenIrs4937391
Biobankrs4937391
1000 genomesrs4937391
hgdprs4937391
ensemblrs4937391
geneviewrs4937391
scholarrs4937391
googlers4937391
pharmgkbrs4937391
gwascentralrs4937391
openSNPrs4937391
23andMers4937391
SNPshotrs4937391
SNPdbers4937391
MSV3drs4937391
GWAS Ctlgrs4937391
GMAF0.2819
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 24382237] Relationship between the G Protein Gated Inward Rectifier Potassium Channel 4 Gene Polymorphism and Dyslipidemia of Uyghur Residents


[PMID 22645387] Influence of age on the association of GIRK4 with metabolic syndrome.


ClinVar
Risk rs4937391(A;A)
Alt rs4937391(A;A)
Reference Rs4937391(G;G)
Significance Non-pathogenic
Disease not specified Familial hyperaldosteronism Romano-Ward syndrome
Variation info
Gene KCNJ5
CLNDBN not specified Familial hyperaldosteronism Romano-Ward syndrome
Reversed 0
HGVS NC_000011.9:g.128786294G>A
CLNSRC ClinVar GeneDx
CLNACC RCV000126426.4, RCV000305432.1, RCV000341556.1,