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rs193922285

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922285(G;T)
Make rs193922285(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145148
GeneGCK
is asnp
is mentioned by
dbSNPrs193922285
ebirs193922285
HLIrs193922285
Exacrs193922285
Varsomers193922285
Maprs193922285
PheGenIrs193922285
hapmaprs193922285
1000 genomesrs193922285
hgdprs193922285
ensemblrs193922285
gopubmedrs193922285
geneviewrs193922285
scholarrs193922285
googlers193922285
pharmgkbrs193922285
gwascentralrs193922285
openSNPrs193922285
23andMers193922285
23andMe allrs193922285
SNP Nexus

SNPshotrs193922285
SNPdbers193922285
MSV3drs193922285
GWAS Ctlgrs193922285
Max Magnitude0
ClinVar
Risk rs193922285(A,T;A,T)
Alt rs193922285(A,T;A,T)
Reference rs193922285(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.44184747C>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029865.1,