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rs193922303

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922303(G;T)
Make rs193922303(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44150039
GeneGCK
is asnp
is mentioned by
dbSNPrs193922303
ebirs193922303
HLIrs193922303
Exacrs193922303
Varsomers193922303
Maprs193922303
PheGenIrs193922303
hapmaprs193922303
1000 genomesrs193922303
hgdprs193922303
ensemblrs193922303
gopubmedrs193922303
geneviewrs193922303
scholarrs193922303
googlers193922303
pharmgkbrs193922303
gwascentralrs193922303
openSNPrs193922303
23andMers193922303
23andMe allrs193922303
SNP Nexus

SNPshotrs193922303
SNPdbers193922303
MSV3drs193922303
GWAS Ctlgrs193922303
Max Magnitude0
ClinVar
Risk rs193922303(T;T)
Alt rs193922303(T;T)
Reference rs193922303(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.44189638C>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029888.1,