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rs193922267

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922267(A;A)
Make rs193922267(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145597
GeneGCK
is asnp
is mentioned by
dbSNPrs193922267
ebirs193922267
HLIrs193922267
Exacrs193922267
Varsomers193922267
Maprs193922267
PheGenIrs193922267
hapmaprs193922267
1000 genomesrs193922267
hgdprs193922267
ensemblrs193922267
gopubmedrs193922267
geneviewrs193922267
scholarrs193922267
googlers193922267
pharmgkbrs193922267
gwascentralrs193922267
openSNPrs193922267
23andMers193922267
23andMe allrs193922267
SNP Nexus

SNPshotrs193922267
SNPdbers193922267
MSV3drs193922267
GWAS Ctlgrs193922267
Max Magnitude0
ClinVar
Risk rs193922267(A;A)
Alt rs193922267(A;A)
Reference rs193922267(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.44185196C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029842.1,