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rs193922290

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922290(A;T)
Make rs193922290(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44152381
GeneGCK
is asnp
is mentioned by
dbSNPrs193922290
ebirs193922290
HLIrs193922290
Exacrs193922290
Varsomers193922290
Maprs193922290
PheGenIrs193922290
hapmaprs193922290
1000 genomesrs193922290
hgdprs193922290
ensemblrs193922290
gopubmedrs193922290
geneviewrs193922290
scholarrs193922290
googlers193922290
pharmgkbrs193922290
gwascentralrs193922290
openSNPrs193922290
23andMers193922290
23andMe allrs193922290
SNP Nexus

SNPshotrs193922290
SNPdbers193922290
MSV3drs193922290
GWAS Ctlgrs193922290
Max Magnitude0
ClinVar
Risk rs193922290(T;T)
Alt rs193922290(T;T)
Reference rs193922290(A;A)
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.44191980T>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029873.1,