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rs193922281

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922281(C;G)
Make rs193922281(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145195
GeneGCK
is asnp
is mentioned by
dbSNPrs193922281
ebirs193922281
HLIrs193922281
Exacrs193922281
Varsomers193922281
Maprs193922281
PheGenIrs193922281
hapmaprs193922281
1000 genomesrs193922281
hgdprs193922281
ensemblrs193922281
gopubmedrs193922281
geneviewrs193922281
scholarrs193922281
googlers193922281
pharmgkbrs193922281
gwascentralrs193922281
openSNPrs193922281
23andMers193922281
23andMe allrs193922281
SNP Nexus

SNPshotrs193922281
SNPdbers193922281
MSV3drs193922281
GWAS Ctlgrs193922281
Max Magnitude0
ClinVar
Risk rs193922281(G;G)
Alt rs193922281(G;G)
Reference rs193922281(C;C)
Significance Probable-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.44184794G>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029861.1,