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rs193922277

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922277(C;C)
Make rs193922277(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145245
GeneGCK
is asnp
is mentioned by
dbSNPrs193922277
ebirs193922277
HLIrs193922277
Exacrs193922277
Varsomers193922277
Maprs193922277
PheGenIrs193922277
hapmaprs193922277
1000 genomesrs193922277
hgdprs193922277
ensemblrs193922277
gopubmedrs193922277
geneviewrs193922277
scholarrs193922277
googlers193922277
pharmgkbrs193922277
gwascentralrs193922277
openSNPrs193922277
23andMers193922277
23andMe allrs193922277
SNP Nexus

SNPshotrs193922277
SNPdbers193922277
MSV3drs193922277
GWAS Ctlgrs193922277
Max Magnitude0
ClinVar
Risk rs193922277(C;C)
Alt rs193922277(C;C)
Reference rs193922277(T;T)
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.44184844A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029857.1,