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rs587783669

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783669(C;G)
Make rs587783669(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position17387594
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs587783669
ebirs587783669
HLIrs587783669
Exacrs587783669
Varsomers587783669
Maprs587783669
PheGenIrs587783669
hapmaprs587783669
1000 genomesrs587783669
hgdprs587783669
ensemblrs587783669
gopubmedrs587783669
geneviewrs587783669
scholarrs587783669
googlers587783669
pharmgkbrs587783669
gwascentralrs587783669
openSNPrs587783669
23andMers587783669
23andMe allrs587783669
SNP Nexus

SNPshotrs587783669
SNPdbers587783669
MSV3drs587783669
GWAS Ctlgrs587783669
Max Magnitude0
ClinVar
Risk rs587783669(G;G)
Alt rs587783669(G;G)
Reference rs587783669(C;C)
Significance Probable-Pathogenic
Disease Diabetes mellitus
Variation info
Gene KCNJ11
CLNDBN Diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17409141G>C
CLNSRC
CLNACC RCV000146107.1,