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rs193922332

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922332(C;C)
Make rs193922332(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44147701
GeneGCK
is asnp
is mentioned by
dbSNPrs193922332
ebirs193922332
HLIrs193922332
Exacrs193922332
Varsomers193922332
Maprs193922332
PheGenIrs193922332
hapmaprs193922332
1000 genomesrs193922332
hgdprs193922332
ensemblrs193922332
gopubmedrs193922332
geneviewrs193922332
scholarrs193922332
googlers193922332
pharmgkbrs193922332
gwascentralrs193922332
openSNPrs193922332
23andMers193922332
23andMe allrs193922332
SNP Nexus

SNPshotrs193922332
SNPdbers193922332
MSV3drs193922332
GWAS Ctlgrs193922332
Max Magnitude0
ClinVar
Risk rs193922332(C;C)
Alt rs193922332(C;C)
Reference rs193922332(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.44187300A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029922.1,