rs4937391

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs4937391(A;A)

Make rs4937391(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

128916399

Gene

KCNJ5

is a	snp
is	mentioned by
dbSNP	rs4937391
dbSNP (classic)	rs4937391
ClinGen	rs4937391
ebi	rs4937391
HLI	rs4937391
Exac	rs4937391
Gnomad	rs4937391
Varsome	rs4937391
LitVar	rs4937391
Map	rs4937391
PheGenI	rs4937391
Biobank	rs4937391
1000 genomes	rs4937391
hgdp	rs4937391
ensembl	rs4937391
geneview	rs4937391
scholar	rs4937391
google	rs4937391
pharmgkb	rs4937391
gwascentral	rs4937391
openSNP	rs4937391
23andMe	rs4937391
SNPshot	rs4937391
SNPdbe	rs4937391
MSV3d	rs4937391
GWAS Ctlg	rs4937391

GMAF

0.2819

Max Magnitude

0

?	(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,