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rs193922325

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922325(G;G)
Make rs193922325(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44153435
GeneGCK
is asnp
is mentioned by
dbSNPrs193922325
ebirs193922325
HLIrs193922325
Exacrs193922325
Varsomers193922325
Maprs193922325
PheGenIrs193922325
hapmaprs193922325
1000 genomesrs193922325
hgdprs193922325
ensemblrs193922325
gopubmedrs193922325
geneviewrs193922325
scholarrs193922325
googlers193922325
pharmgkbrs193922325
gwascentralrs193922325
openSNPrs193922325
23andMers193922325
23andMe allrs193922325
SNP Nexus

SNPshotrs193922325
SNPdbers193922325
MSV3drs193922325
GWAS Ctlgrs193922325
Max Magnitude0
ClinVar
Risk rs193922325(G;G)
Alt rs193922325(G;G)
Reference rs193922325(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.44193034A>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029913.1,