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rs193922313

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922313(G;T)
Make rs193922313(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44149809
GeneGCK
is asnp
is mentioned by
dbSNPrs193922313
ebirs193922313
HLIrs193922313
Exacrs193922313
Varsomers193922313
Maprs193922313
PheGenIrs193922313
hapmaprs193922313
1000 genomesrs193922313
hgdprs193922313
ensemblrs193922313
gopubmedrs193922313
geneviewrs193922313
scholarrs193922313
googlers193922313
pharmgkbrs193922313
gwascentralrs193922313
openSNPrs193922313
23andMers193922313
23andMe allrs193922313
SNP Nexus

SNPshotrs193922313
SNPdbers193922313
MSV3drs193922313
GWAS Ctlgrs193922313
Max Magnitude0
ClinVar
Risk rs193922313(T;T)
Alt rs193922313(T;T)
Reference rs193922313(G;G)
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.44189408C>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029899.1,