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rs104894011

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 2 associated with MODY2; maturity onset of diabetes in the young (type 2)
Make rs104894011(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44147720
GeneGCK
is asnp
is mentioned by
dbSNPrs104894011
ebirs104894011
HLIrs104894011
Exacrs104894011
Varsomers104894011
Maprs104894011
PheGenIrs104894011
hapmaprs104894011
1000 genomesrs104894011
hgdprs104894011
ensemblrs104894011
gopubmedrs104894011
geneviewrs104894011
scholarrs104894011
googlers104894011
pharmgkbrs104894011
gwascentralrs104894011
openSNPrs104894011
23andMers104894011
23andMe allrs104894011
SNP Nexus

SNPshotrs104894011
SNPdbers104894011
MSV3drs104894011
GWAS Ctlgrs104894011
Max Magnitude2
OMIM138079
Desc
Variant0008
Relatedalso
ClinVar
Risk rs104894011(T;T)
Alt rs104894011(T;T)
Reference rs104894011(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.44187319C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017519.24,