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rs193922295

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922295(-;-)
Make rs193922295(-;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position44151046
GeneGCK
is asnp
is mentioned by
dbSNPrs193922295
ebirs193922295
HLIrs193922295
Exacrs193922295
Varsomers193922295
Maprs193922295
PheGenIrs193922295
hapmaprs193922295
1000 genomesrs193922295
hgdprs193922295
ensemblrs193922295
gopubmedrs193922295
geneviewrs193922295
scholarrs193922295
googlers193922295
pharmgkbrs193922295
gwascentralrs193922295
openSNPrs193922295
23andMers193922295
23andMe allrs193922295
SNP Nexus

SNPshotrs193922295
SNPdbers193922295
MSV3drs193922295
GWAS Ctlgrs193922295
Max Magnitude0
ClinVar
Risk rs193922295(;)
Alt rs193922295(;)
Reference rs193922295(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.44190645delG
CLNSRC ClinVar LabCorp
CLNACC RCV000029879.1,