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rs193922261

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922261(C;C)
Make rs193922261(C;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44153402
GeneGCK
is asnp
is mentioned by
dbSNPrs193922261
ebirs193922261
HLIrs193922261
Exacrs193922261
Varsomers193922261
Maprs193922261
PheGenIrs193922261
hapmaprs193922261
1000 genomesrs193922261
hgdprs193922261
ensemblrs193922261
gopubmedrs193922261
geneviewrs193922261
scholarrs193922261
googlers193922261
pharmgkbrs193922261
gwascentralrs193922261
openSNPrs193922261
23andMers193922261
23andMe allrs193922261
SNP Nexus

SNPshotrs193922261
SNPdbers193922261
MSV3drs193922261
GWAS Ctlgrs193922261
Max Magnitude0
ClinVar
Risk rs193922261(C;C)
Alt rs193922261(C;C)
Reference rs193922261(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.44193001C>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029836.1,