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rs193922269

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922269(G;T)
Make rs193922269(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145575
GeneGCK
is asnp
is mentioned by
dbSNPrs193922269
ebirs193922269
HLIrs193922269
Exacrs193922269
Varsomers193922269
Maprs193922269
PheGenIrs193922269
hapmaprs193922269
1000 genomesrs193922269
hgdprs193922269
ensemblrs193922269
gopubmedrs193922269
geneviewrs193922269
scholarrs193922269
googlers193922269
pharmgkbrs193922269
gwascentralrs193922269
openSNPrs193922269
23andMers193922269
23andMe allrs193922269
SNP Nexus

SNPshotrs193922269
SNPdbers193922269
MSV3drs193922269
GWAS Ctlgrs193922269
Max Magnitude0
ClinVar
Risk rs193922269(T;T)
Alt rs193922269(T;T)
Reference rs193922269(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.44185174C>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029848.1,