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rs587780346

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587780346(A;C)
Make rs587780346(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position44149823
GeneGCK, LOC105375258
is asnp
is mentioned by
dbSNPrs587780346
ebirs587780346
HLIrs587780346
Exacrs587780346
Varsomers587780346
Maprs587780346
PheGenIrs587780346
hapmaprs587780346
1000 genomesrs587780346
hgdprs587780346
ensemblrs587780346
gopubmedrs587780346
geneviewrs587780346
scholarrs587780346
googlers587780346
pharmgkbrs587780346
gwascentralrs587780346
openSNPrs587780346
23andMers587780346
23andMe allrs587780346
SNP Nexus

SNPshotrs587780346
SNPdbers587780346
MSV3drs587780346
GWAS Ctlgrs587780346
Max Magnitude0
ClinVar
Risk rs587780346(C;C)
Alt rs587780346(C;C)
Reference rs587780346(A;A)
Significance Probable-Pathogenic
Disease Diabetes mellitus
Variation info
Gene GCK
CLNDBN Diabetes mellitus, gestational
Reversed 1
HGVS NC_000007.13:g.44189422T>G
CLNSRC
CLNACC RCV000117132.1,