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rs193922286

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922286(A;A)
Make rs193922286(A;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position44153363
GeneGCK
is asnp
is mentioned by
dbSNPrs193922286
ebirs193922286
HLIrs193922286
Exacrs193922286
Varsomers193922286
Maprs193922286
PheGenIrs193922286
hapmaprs193922286
1000 genomesrs193922286
hgdprs193922286
ensemblrs193922286
gopubmedrs193922286
geneviewrs193922286
scholarrs193922286
googlers193922286
pharmgkbrs193922286
gwascentralrs193922286
openSNPrs193922286
23andMers193922286
23andMe allrs193922286
SNP Nexus

SNPshotrs193922286
SNPdbers193922286
MSV3drs193922286
GWAS Ctlgrs193922286
Max Magnitude0
ClinVar
Risk rs193922286(A;A)
Alt rs193922286(A;A)
Reference rs193922286(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.44192962G>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029867.1,