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rs587780343

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780343(G;T)
Make rs587780343(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position44145638
GeneGCK
is asnp
is mentioned by
dbSNPrs587780343
ebirs587780343
HLIrs587780343
Exacrs587780343
Varsomers587780343
Maprs587780343
PheGenIrs587780343
hapmaprs587780343
1000 genomesrs587780343
hgdprs587780343
ensemblrs587780343
gopubmedrs587780343
geneviewrs587780343
scholarrs587780343
googlers587780343
pharmgkbrs587780343
gwascentralrs587780343
openSNPrs587780343
23andMers587780343
23andMe allrs587780343
SNP Nexus

SNPshotrs587780343
SNPdbers587780343
MSV3drs587780343
GWAS Ctlgrs587780343
Max Magnitude0
ClinVar
Risk rs587780343(T;T)
Alt rs587780343(T;T)
Reference rs587780343(G;G)
Significance Probable-Pathogenic
Disease Diabetes mellitus
Variation info
Gene GCK
CLNDBN Diabetes mellitus, gestational
Reversed 1
HGVS NC_000007.13:g.44185237C>A
CLNSRC
CLNACC RCV000117127.1,