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rs587783670

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783670(C;G)
Make rs587783670(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position17387571
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs587783670
ebirs587783670
HLIrs587783670
Exacrs587783670
Varsomers587783670
Maprs587783670
PheGenIrs587783670
hapmaprs587783670
1000 genomesrs587783670
hgdprs587783670
ensemblrs587783670
gopubmedrs587783670
geneviewrs587783670
scholarrs587783670
googlers587783670
pharmgkbrs587783670
gwascentralrs587783670
openSNPrs587783670
23andMers587783670
23andMe allrs587783670
SNP Nexus

SNPshotrs587783670
SNPdbers587783670
MSV3drs587783670
GWAS Ctlgrs587783670
Max Magnitude0
ClinVar
Risk rs587783670(G;G)
Alt rs587783670(G;G)
Reference rs587783670(C;C)
Significance Pathogenic
Disease Neonatal insulin-dependent diabetes mellitus
Variation info
Gene KCNJ11
CLNDBN Neonatal insulin-dependent diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17409118G>C
CLNSRC
CLNACC RCV000146108.1,