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rs193922273

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922273(A;A)
Make rs193922273(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145266
GeneGCK
is asnp
is mentioned by
dbSNPrs193922273
ebirs193922273
HLIrs193922273
Exacrs193922273
Varsomers193922273
Maprs193922273
PheGenIrs193922273
hapmaprs193922273
1000 genomesrs193922273
hgdprs193922273
ensemblrs193922273
gopubmedrs193922273
geneviewrs193922273
scholarrs193922273
googlers193922273
pharmgkbrs193922273
gwascentralrs193922273
openSNPrs193922273
23andMers193922273
23andMe allrs193922273
SNP Nexus

SNPshotrs193922273
SNPdbers193922273
MSV3drs193922273
GWAS Ctlgrs193922273
Max Magnitude0
ClinVar
Risk rs193922273(A;A)
Alt rs193922273(A;A)
Reference rs193922273(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.44184865A>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029852.1,