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rs193922333

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922333(A;T)
Make rs193922333(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44147680
GeneGCK
is asnp
is mentioned by
dbSNPrs193922333
ebirs193922333
HLIrs193922333
Exacrs193922333
Varsomers193922333
Maprs193922333
PheGenIrs193922333
hapmaprs193922333
1000 genomesrs193922333
hgdprs193922333
ensemblrs193922333
gopubmedrs193922333
geneviewrs193922333
scholarrs193922333
googlers193922333
pharmgkbrs193922333
gwascentralrs193922333
openSNPrs193922333
23andMers193922333
23andMe allrs193922333
SNP Nexus

SNPshotrs193922333
SNPdbers193922333
MSV3drs193922333
GWAS Ctlgrs193922333
Max Magnitude0
ClinVar
Risk rs193922333(T;T)
Alt rs193922333(T;T)
Reference rs193922333(A;A)
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.44187279T>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029923.1,