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rs587777439

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777439(A;A)
Make rs587777439(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position128912009
GeneKCNJ5
is asnp
is mentioned by
dbSNPrs587777439
ebirs587777439
HLIrs587777439
Exacrs587777439
Varsomers587777439
Maprs587777439
PheGenIrs587777439
hapmaprs587777439
1000 genomesrs587777439
hgdprs587777439
ensemblrs587777439
gopubmedrs587777439
geneviewrs587777439
scholarrs587777439
googlers587777439
pharmgkbrs587777439
gwascentralrs587777439
openSNPrs587777439
23andMers587777439
23andMe allrs587777439
SNP Nexus

SNPshotrs587777439
SNPdbers587777439
MSV3drs587777439
GWAS Ctlgrs587777439
Max Magnitude0
ClinVar
Risk rs587777439(A;A)
Alt rs587777439(A;A)
Reference rs587777439(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.128781904G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000122753.2,