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rs587783672

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783672(A;A)
Make rs587783672(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position17387413
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs587783672
ebirs587783672
HLIrs587783672
Exacrs587783672
Varsomers587783672
Maprs587783672
PheGenIrs587783672
hapmaprs587783672
1000 genomesrs587783672
hgdprs587783672
ensemblrs587783672
gopubmedrs587783672
geneviewrs587783672
scholarrs587783672
googlers587783672
pharmgkbrs587783672
gwascentralrs587783672
openSNPrs587783672
23andMers587783672
23andMe allrs587783672
SNP Nexus

SNPshotrs587783672
SNPdbers587783672
MSV3drs587783672
GWAS Ctlgrs587783672
Max Magnitude0
ClinVar
Risk rs587783672(A;A)
Alt rs587783672(A;A)
Reference rs587783672(G;G)
Significance Pathogenic
Disease Diabetes mellitus Maturity-onset diabetes of the young
Variation info
Gene KCNJ11
CLNDBN Diabetes mellitus Maturity-onset diabetes of the young, type 13
Reversed 1
HGVS NC_000011.9:g.17408960C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000146115.1, RCV000170299.3,