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rs193922282

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922282(A;A)
Make rs193922282(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145189
GeneGCK
is asnp
is mentioned by
dbSNPrs193922282
ebirs193922282
HLIrs193922282
Exacrs193922282
Varsomers193922282
Maprs193922282
PheGenIrs193922282
hapmaprs193922282
1000 genomesrs193922282
hgdprs193922282
ensemblrs193922282
gopubmedrs193922282
geneviewrs193922282
scholarrs193922282
googlers193922282
pharmgkbrs193922282
gwascentralrs193922282
openSNPrs193922282
23andMers193922282
23andMe allrs193922282
SNP Nexus

SNPshotrs193922282
SNPdbers193922282
MSV3drs193922282
GWAS Ctlgrs193922282
Max Magnitude0
ClinVar
Risk rs193922282(A;A)
Alt rs193922282(A;A)
Reference rs193922282(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.44184788C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029862.1,