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rs878853246

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853246(C;T)
Make rs878853246(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position44153397
GeneGCK
is asnp
is mentioned by
dbSNPrs878853246
ebirs878853246
HLIrs878853246
Exacrs878853246
Varsomers878853246
Maprs878853246
PheGenIrs878853246
hapmaprs878853246
1000 genomesrs878853246
hgdprs878853246
ensemblrs878853246
gopubmedrs878853246
geneviewrs878853246
scholarrs878853246
googlers878853246
pharmgkbrs878853246
gwascentralrs878853246
openSNPrs878853246
23andMers878853246
23andMe allrs878853246
SNP Nexus

SNPshotrs878853246
SNPdbers878853246
MSV3drs878853246
GWAS Ctlgrs878853246
Max Magnitude0
ClinVar
Risk rs878853246(T;T)
Alt rs878853246(T;T)
Reference rs878853246(C;C)
Significance Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene GCK
CLNDBN Maturity-onset diabetes of the young, type 2
Reversed 1
HGVS NC_000007.13:g.44192996G>A
CLNSRC
CLNACC RCV000225041.1,