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rs587777437

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777437(A;A)
Make rs587777437(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position128911725
GeneKCNJ5
is asnp
is mentioned by
dbSNPrs587777437
ebirs587777437
HLIrs587777437
Exacrs587777437
Varsomers587777437
Maprs587777437
PheGenIrs587777437
hapmaprs587777437
1000 genomesrs587777437
hgdprs587777437
ensemblrs587777437
gopubmedrs587777437
geneviewrs587777437
scholarrs587777437
googlers587777437
pharmgkbrs587777437
gwascentralrs587777437
openSNPrs587777437
23andMers587777437
23andMe allrs587777437
SNP Nexus

SNPshotrs587777437
SNPdbers587777437
MSV3drs587777437
GWAS Ctlgrs587777437
Max Magnitude0
ClinVar
Risk rs587777437(A;A)
Alt rs587777437(A;A)
Reference rs587777437(G;G)
Significance Pathogenic
Disease Familial hyperaldosteronism type 3
Variation info
Gene KCNJ5
CLNDBN Familial hyperaldosteronism type 3
Reversed 0
HGVS NC_000011.9:g.128781620G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000122751.2,