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rs193922322

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922322(A;A)
Make rs193922322(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44147819
GeneGCK
is asnp
is mentioned by
dbSNPrs193922322
ebirs193922322
HLIrs193922322
Exacrs193922322
Varsomers193922322
Maprs193922322
PheGenIrs193922322
hapmaprs193922322
1000 genomesrs193922322
hgdprs193922322
ensemblrs193922322
gopubmedrs193922322
geneviewrs193922322
scholarrs193922322
googlers193922322
pharmgkbrs193922322
gwascentralrs193922322
openSNPrs193922322
23andMers193922322
23andMe allrs193922322
SNP Nexus

SNPshotrs193922322
SNPdbers193922322
MSV3drs193922322
GWAS Ctlgrs193922322
Max Magnitude0
ClinVar
Risk rs193922322(A;A)
Alt rs193922322(A;A)
Reference rs193922322(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.44187418C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029910.1,