Have questions? Visit https://www.reddit.com/r/SNPedia

rs193922326

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922326(C;C)
Make rs193922326(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44147761
GeneGCK
is asnp
is mentioned by
dbSNPrs193922326
ebirs193922326
HLIrs193922326
Exacrs193922326
Varsomers193922326
Maprs193922326
PheGenIrs193922326
hapmaprs193922326
1000 genomesrs193922326
hgdprs193922326
ensemblrs193922326
gopubmedrs193922326
geneviewrs193922326
scholarrs193922326
googlers193922326
pharmgkbrs193922326
gwascentralrs193922326
openSNPrs193922326
23andMers193922326
23andMe allrs193922326
SNP Nexus

SNPshotrs193922326
SNPdbers193922326
MSV3drs193922326
GWAS Ctlgrs193922326
Max Magnitude0
ClinVar
Risk rs193922326(C;C)
Alt rs193922326(C;C)
Reference rs193922326(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.44187360A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029914.1,