Have questions? Visit https://www.reddit.com/r/SNPedia

rs193922337

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922337(C;C)
Make rs193922337(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44146565
GeneGCK
is asnp
is mentioned by
dbSNPrs193922337
ebirs193922337
HLIrs193922337
Exacrs193922337
Varsomers193922337
Maprs193922337
PheGenIrs193922337
hapmaprs193922337
1000 genomesrs193922337
hgdprs193922337
ensemblrs193922337
gopubmedrs193922337
geneviewrs193922337
scholarrs193922337
googlers193922337
pharmgkbrs193922337
gwascentralrs193922337
openSNPrs193922337
23andMers193922337
23andMe allrs193922337
SNP Nexus

SNPshotrs193922337
SNPdbers193922337
MSV3drs193922337
GWAS Ctlgrs193922337
Max Magnitude0
ClinVar
Risk rs193922337(C;C)
Alt rs193922337(C;C)
Reference rs193922337(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.44186164A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029928.1,