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rs104894016

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;G) 2 associated with MODY2; maturity onset of diabetes in the young (type 2)
(G;G) 0 common in clinvar


Make rs104894016(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145618
GeneGCK
is asnp
is mentioned by
dbSNPrs104894016
ebirs104894016
HLIrs104894016
Exacrs104894016
Varsomers104894016
Maprs104894016
PheGenIrs104894016
hapmaprs104894016
1000 genomesrs104894016
hgdprs104894016
ensemblrs104894016
gopubmedrs104894016
geneviewrs104894016
scholarrs104894016
googlers104894016
pharmgkbrs104894016
gwascentralrs104894016
openSNPrs104894016
23andMers104894016
23andMe allrs104894016
SNP Nexus

SNPshotrs104894016
SNPdbers104894016
MSV3drs104894016
GWAS Ctlgrs104894016
Max Magnitude2
OMIM138079
Desc
Variant0014
Relatedalso
ClinVar
Risk rs104894016(A;A)
Alt rs104894016(A;A)
Reference rs104894016(G;G)
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.44185217C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017527.29,