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rs193922280

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922280(-;-)
Make rs193922280(-;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145202
GeneGCK
is asnp
is mentioned by
dbSNPrs193922280
ebirs193922280
HLIrs193922280
Exacrs193922280
Varsomers193922280
Maprs193922280
PheGenIrs193922280
hapmaprs193922280
1000 genomesrs193922280
hgdprs193922280
ensemblrs193922280
gopubmedrs193922280
geneviewrs193922280
scholarrs193922280
googlers193922280
pharmgkbrs193922280
gwascentralrs193922280
openSNPrs193922280
23andMers193922280
23andMe allrs193922280
SNP Nexus

SNPshotrs193922280
SNPdbers193922280
MSV3drs193922280
GWAS Ctlgrs193922280
Max Magnitude0
ClinVar
Risk rs193922280(;)
Alt rs193922280(;)
Reference rs193922280(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.44184801delG
CLNSRC ClinVar LabCorp
CLNACC RCV000029860.1,