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rs193922339

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922339(A;A)
Make rs193922339(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44146535
GeneGCK
is asnp
is mentioned by
dbSNPrs193922339
ebirs193922339
HLIrs193922339
Exacrs193922339
Varsomers193922339
Maprs193922339
PheGenIrs193922339
hapmaprs193922339
1000 genomesrs193922339
hgdprs193922339
ensemblrs193922339
gopubmedrs193922339
geneviewrs193922339
scholarrs193922339
googlers193922339
pharmgkbrs193922339
gwascentralrs193922339
openSNPrs193922339
23andMers193922339
23andMe allrs193922339
SNP Nexus

SNPshotrs193922339
SNPdbers193922339
MSV3drs193922339
GWAS Ctlgrs193922339
Max Magnitude0
ClinVar
Risk rs193922339(A;A)
Alt rs193922339(A;A)
Reference rs193922339(T;T)
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.44186134A>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029930.1,