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rs193922263

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922263(C;T)
Make rs193922263(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145626
GeneGCK
is asnp
is mentioned by
dbSNPrs193922263
ebirs193922263
HLIrs193922263
Exacrs193922263
Varsomers193922263
Maprs193922263
PheGenIrs193922263
hapmaprs193922263
1000 genomesrs193922263
hgdprs193922263
ensemblrs193922263
gopubmedrs193922263
geneviewrs193922263
scholarrs193922263
googlers193922263
pharmgkbrs193922263
gwascentralrs193922263
openSNPrs193922263
23andMers193922263
23andMe allrs193922263
SNP Nexus

SNPshotrs193922263
SNPdbers193922263
MSV3drs193922263
GWAS Ctlgrs193922263
Max Magnitude0
ClinVar
Risk rs193922263(T;T)
Alt rs193922263(T;T)
Reference rs193922263(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.44185225G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029838.1,