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rs587783675

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783675(C;C)
Make rs587783675(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position17387104
GeneKCNJ11
is asnp
is mentioned by
dbSNPrs587783675
ebirs587783675
HLIrs587783675
Exacrs587783675
Varsomers587783675
Maprs587783675
PheGenIrs587783675
hapmaprs587783675
1000 genomesrs587783675
hgdprs587783675
ensemblrs587783675
gopubmedrs587783675
geneviewrs587783675
scholarrs587783675
googlers587783675
pharmgkbrs587783675
gwascentralrs587783675
openSNPrs587783675
23andMers587783675
23andMe allrs587783675
SNP Nexus

SNPshotrs587783675
SNPdbers587783675
MSV3drs587783675
GWAS Ctlgrs587783675
Max Magnitude0
ClinVar
Risk rs587783675(C;C)
Alt rs587783675(C;C)
Reference rs587783675(T;T)
Significance Pathogenic
Disease Diabetes mellitus
Variation info
Gene KCNJ11
CLNDBN Diabetes mellitus
Reversed 1
HGVS NC_000011.9:g.17408651A>G
CLNSRC
CLNACC RCV000146123.1,