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rs193922302

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922302(A;A)
Make rs193922302(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44150956
GeneGCK
is asnp
is mentioned by
dbSNPrs193922302
ebirs193922302
HLIrs193922302
Exacrs193922302
Varsomers193922302
Maprs193922302
PheGenIrs193922302
hapmaprs193922302
1000 genomesrs193922302
hgdprs193922302
ensemblrs193922302
gopubmedrs193922302
geneviewrs193922302
scholarrs193922302
googlers193922302
pharmgkbrs193922302
gwascentralrs193922302
openSNPrs193922302
23andMers193922302
23andMe allrs193922302
SNP Nexus

SNPshotrs193922302
SNPdbers193922302
MSV3drs193922302
GWAS Ctlgrs193922302
Max Magnitude0
ClinVar
Risk rs193922302(A;A)
Alt rs193922302(A;A)
Reference rs193922302(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.44190555C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029887.1,


[PMID 19564454OA-icon.png] Maturity-onset diabetes of the young in children with incidental hyperglycemia: a multicenter Italian study of 172 families.