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rs193922266

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922266(G;G)
Make rs193922266(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145608
GeneGCK
is asnp
is mentioned by
dbSNPrs193922266
ebirs193922266
HLIrs193922266
Exacrs193922266
Varsomers193922266
Maprs193922266
PheGenIrs193922266
hapmaprs193922266
1000 genomesrs193922266
hgdprs193922266
ensemblrs193922266
gopubmedrs193922266
geneviewrs193922266
scholarrs193922266
googlers193922266
pharmgkbrs193922266
gwascentralrs193922266
openSNPrs193922266
23andMers193922266
23andMe allrs193922266
SNP Nexus

SNPshotrs193922266
SNPdbers193922266
MSV3drs193922266
GWAS Ctlgrs193922266
Max Magnitude0
ClinVar
Risk rs193922266(G;G)
Alt rs193922266(G;G)
Reference rs193922266(T;T)
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.44185207A>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029841.1,