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rs193922260

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922260(A;T)
Make rs193922260(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145708
GeneGCK
is asnp
is mentioned by
dbSNPrs193922260
ebirs193922260
HLIrs193922260
Exacrs193922260
Varsomers193922260
Maprs193922260
PheGenIrs193922260
hapmaprs193922260
1000 genomesrs193922260
hgdprs193922260
ensemblrs193922260
gopubmedrs193922260
geneviewrs193922260
scholarrs193922260
googlers193922260
pharmgkbrs193922260
gwascentralrs193922260
openSNPrs193922260
23andMers193922260
23andMe allrs193922260
SNP Nexus

SNPshotrs193922260
SNPdbers193922260
MSV3drs193922260
GWAS Ctlgrs193922260
Max Magnitude0
ClinVar
Risk rs193922260(T;T)
Alt rs193922260(T;T)
Reference rs193922260(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.44185307T>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029835.1,