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rs193922327

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922327(A;C)
Make rs193922327(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position44147753
GeneGCK
is asnp
is mentioned by
dbSNPrs193922327
ebirs193922327
HLIrs193922327
Exacrs193922327
Varsomers193922327
Maprs193922327
PheGenIrs193922327
hapmaprs193922327
1000 genomesrs193922327
hgdprs193922327
ensemblrs193922327
gopubmedrs193922327
geneviewrs193922327
scholarrs193922327
googlers193922327
pharmgkbrs193922327
gwascentralrs193922327
openSNPrs193922327
23andMers193922327
23andMe allrs193922327
SNP Nexus

SNPshotrs193922327
SNPdbers193922327
MSV3drs193922327
GWAS Ctlgrs193922327
Max Magnitude0
ClinVar
Risk rs193922327(C;C)
Alt rs193922327(C;C)
Reference rs193922327(A;A)
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.44187352T>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029917.1,