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rs587777438

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777438(G;G)
Make rs587777438(G;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position128911743
GeneKCNJ5
is asnp
is mentioned by
dbSNPrs587777438
ebirs587777438
HLIrs587777438
Exacrs587777438
Varsomers587777438
Maprs587777438
PheGenIrs587777438
hapmaprs587777438
1000 genomesrs587777438
hgdprs587777438
ensemblrs587777438
gopubmedrs587777438
geneviewrs587777438
scholarrs587777438
googlers587777438
pharmgkbrs587777438
gwascentralrs587777438
openSNPrs587777438
23andMers587777438
23andMe allrs587777438
SNP Nexus

SNPshotrs587777438
SNPdbers587777438
MSV3drs587777438
GWAS Ctlgrs587777438
Max Magnitude0
ClinVar
Risk rs587777438(G;G)
Alt rs587777438(G;G)
Reference rs587777438(T;T)
Significance Pathogenic
Disease Familial hyperaldosteronism type 3
Variation info
Gene KCNJ5
CLNDBN Familial hyperaldosteronism type 3
Reversed 0
HGVS NC_000011.9:g.128781638T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000122752.2,