rs4937391
From SNPedia
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 |
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, |