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rs193922304

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922304(C;G)
Make rs193922304(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44150021
GeneGCK
is asnp
is mentioned by
dbSNPrs193922304
ebirs193922304
HLIrs193922304
Exacrs193922304
Varsomers193922304
Maprs193922304
PheGenIrs193922304
hapmaprs193922304
1000 genomesrs193922304
hgdprs193922304
ensemblrs193922304
gopubmedrs193922304
geneviewrs193922304
scholarrs193922304
googlers193922304
pharmgkbrs193922304
gwascentralrs193922304
openSNPrs193922304
23andMers193922304
23andMe allrs193922304
SNP Nexus

SNPshotrs193922304
SNPdbers193922304
MSV3drs193922304
GWAS Ctlgrs193922304
Max Magnitude0
ClinVar
Risk rs193922304(G;G)
Alt rs193922304(G;G)
Reference rs193922304(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.44189620G>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029889.1,