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rs587780345

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780345(A;A)
Make rs587780345(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position44150004
GeneGCK, LOC105375258
is asnp
is mentioned by
dbSNPrs587780345
ebirs587780345
HLIrs587780345
Exacrs587780345
Varsomers587780345
Maprs587780345
PheGenIrs587780345
hapmaprs587780345
1000 genomesrs587780345
hgdprs587780345
ensemblrs587780345
gopubmedrs587780345
geneviewrs587780345
scholarrs587780345
googlers587780345
pharmgkbrs587780345
gwascentralrs587780345
openSNPrs587780345
23andMers587780345
23andMe allrs587780345
SNP Nexus

SNPshotrs587780345
SNPdbers587780345
MSV3drs587780345
GWAS Ctlgrs587780345
Max Magnitude0
ClinVar
Risk rs587780345(A;A)
Alt rs587780345(A;A)
Reference rs587780345(G;G)
Significance Pathogenic
Disease Diabetes mellitus
Variation info
Gene GCK
CLNDBN Diabetes mellitus, gestational
Reversed 1
HGVS NC_000007.13:g.44189603C>T
CLNSRC
CLNACC RCV000117131.1,