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rs193922268

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922268(C;C)
Make rs193922268(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145593
GeneGCK
is asnp
is mentioned by
dbSNPrs193922268
ebirs193922268
HLIrs193922268
Exacrs193922268
Varsomers193922268
Maprs193922268
PheGenIrs193922268
hapmaprs193922268
1000 genomesrs193922268
hgdprs193922268
ensemblrs193922268
gopubmedrs193922268
geneviewrs193922268
scholarrs193922268
googlers193922268
pharmgkbrs193922268
gwascentralrs193922268
openSNPrs193922268
23andMers193922268
23andMe allrs193922268
SNP Nexus

SNPshotrs193922268
SNPdbers193922268
MSV3drs193922268
GWAS Ctlgrs193922268
Max Magnitude0
ClinVar
Risk rs193922268(C;C)
Alt rs193922268(C;C)
Reference rs193922268(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.44185192A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029843.1,