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rs587780347

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780347(A;A)
Make rs587780347(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position44147807
GeneGCK, LOC105375258
is asnp
is mentioned by
dbSNPrs587780347
ebirs587780347
HLIrs587780347
Exacrs587780347
Varsomers587780347
Maprs587780347
PheGenIrs587780347
hapmaprs587780347
1000 genomesrs587780347
hgdprs587780347
ensemblrs587780347
gopubmedrs587780347
geneviewrs587780347
scholarrs587780347
googlers587780347
pharmgkbrs587780347
gwascentralrs587780347
openSNPrs587780347
23andMers587780347
23andMe allrs587780347
SNP Nexus

SNPshotrs587780347
SNPdbers587780347
MSV3drs587780347
GWAS Ctlgrs587780347
Max Magnitude0
ClinVar
Risk rs587780347(A;A)
Alt rs587780347(A;A)
Reference rs587780347(G;G)
Significance Pathogenic
Disease Diabetes mellitus
Variation info
Gene GCK
CLNDBN Diabetes mellitus, gestational
Reversed 1
HGVS NC_000007.13:g.44187406C>T
CLNSRC
CLNACC RCV000117134.1,