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rs193922259

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922259(A;T)
Make rs193922259(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44153406
GeneGCK
is asnp
is mentioned by
dbSNPrs193922259
ebirs193922259
HLIrs193922259
Exacrs193922259
Varsomers193922259
Maprs193922259
PheGenIrs193922259
hapmaprs193922259
1000 genomesrs193922259
hgdprs193922259
ensemblrs193922259
gopubmedrs193922259
geneviewrs193922259
scholarrs193922259
googlers193922259
pharmgkbrs193922259
gwascentralrs193922259
openSNPrs193922259
23andMers193922259
23andMe allrs193922259
SNP Nexus

SNPshotrs193922259
SNPdbers193922259
MSV3drs193922259
GWAS Ctlgrs193922259
Max Magnitude0
ClinVar
Risk rs193922259(T;T)
Alt rs193922259(T;T)
Reference rs193922259(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.44193005T>A
CLNSRC ClinVar
CLNACC RCV000029834.1,