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rs193922300

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922300(C;T)
Make rs193922300(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44150982
GeneGCK
is asnp
is mentioned by
dbSNPrs193922300
ebirs193922300
HLIrs193922300
Exacrs193922300
Varsomers193922300
Maprs193922300
PheGenIrs193922300
hapmaprs193922300
1000 genomesrs193922300
hgdprs193922300
ensemblrs193922300
gopubmedrs193922300
geneviewrs193922300
scholarrs193922300
googlers193922300
pharmgkbrs193922300
gwascentralrs193922300
openSNPrs193922300
23andMers193922300
23andMe allrs193922300
SNP Nexus

SNPshotrs193922300
SNPdbers193922300
MSV3drs193922300
GWAS Ctlgrs193922300
Max Magnitude0
ClinVar
Risk rs193922300(T;T)
Alt rs193922300(T;T)
Reference rs193922300(C;C)
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.44190581G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029884.1,