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rs193922296

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922296(A;A)
Make rs193922296(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44150999
GeneGCK
is asnp
is mentioned by
dbSNPrs193922296
ebirs193922296
HLIrs193922296
Exacrs193922296
Varsomers193922296
Maprs193922296
PheGenIrs193922296
hapmaprs193922296
1000 genomesrs193922296
hgdprs193922296
ensemblrs193922296
gopubmedrs193922296
geneviewrs193922296
scholarrs193922296
googlers193922296
pharmgkbrs193922296
gwascentralrs193922296
openSNPrs193922296
23andMers193922296
23andMe allrs193922296
SNP Nexus

SNPshotrs193922296
SNPdbers193922296
MSV3drs193922296
GWAS Ctlgrs193922296
Max Magnitude0
ClinVar
Risk rs193922296(A;A)
Alt rs193922296(A;A)
Reference rs193922296(G;G)
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.44190598C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029880.1,