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rs193922308

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922308(C;G)
Make rs193922308(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44153452
GeneGCK
is asnp
is mentioned by
dbSNPrs193922308
ebirs193922308
HLIrs193922308
Exacrs193922308
Varsomers193922308
Maprs193922308
PheGenIrs193922308
hapmaprs193922308
1000 genomesrs193922308
hgdprs193922308
ensemblrs193922308
gopubmedrs193922308
geneviewrs193922308
scholarrs193922308
googlers193922308
pharmgkbrs193922308
gwascentralrs193922308
openSNPrs193922308
23andMers193922308
23andMe allrs193922308
SNP Nexus

SNPshotrs193922308
SNPdbers193922308
MSV3drs193922308
GWAS Ctlgrs193922308
Max Magnitude0
ClinVar
Risk rs193922308(G;G)
Alt rs193922308(G;G)
Reference rs193922308(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.44193051G>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029893.1,