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rs193922292

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922292(G;G)
Make rs193922292(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44152312
GeneGCK
is asnp
is mentioned by
dbSNPrs193922292
ebirs193922292
HLIrs193922292
Exacrs193922292
Varsomers193922292
Maprs193922292
PheGenIrs193922292
hapmaprs193922292
1000 genomesrs193922292
hgdprs193922292
ensemblrs193922292
gopubmedrs193922292
geneviewrs193922292
scholarrs193922292
googlers193922292
pharmgkbrs193922292
gwascentralrs193922292
openSNPrs193922292
23andMers193922292
23andMe allrs193922292
SNP Nexus

SNPshotrs193922292
SNPdbers193922292
MSV3drs193922292
GWAS Ctlgrs193922292
Max Magnitude0
ClinVar
Risk rs193922292(G;G)
Alt rs193922292(G;G)
Reference rs193922292(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.44191911A>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029875.1,