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rs193922287

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922287(C;T)
Make rs193922287(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44153334
GeneGCK
is asnp
is mentioned by
dbSNPrs193922287
ebirs193922287
HLIrs193922287
Exacrs193922287
Varsomers193922287
Maprs193922287
PheGenIrs193922287
hapmaprs193922287
1000 genomesrs193922287
hgdprs193922287
ensemblrs193922287
gopubmedrs193922287
geneviewrs193922287
scholarrs193922287
googlers193922287
pharmgkbrs193922287
gwascentralrs193922287
openSNPrs193922287
23andMers193922287
23andMe allrs193922287
SNP Nexus

SNPshotrs193922287
SNPdbers193922287
MSV3drs193922287
GWAS Ctlgrs193922287
Max Magnitude0
ClinVar
Risk rs193922287(T;T)
Alt rs193922287(T;T)
Reference rs193922287(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.44192933G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029868.1,