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rs193922291

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922291(A;T)
Make rs193922291(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44152330
GeneGCK
is asnp
is mentioned by
dbSNPrs193922291
ebirs193922291
HLIrs193922291
Exacrs193922291
Varsomers193922291
Maprs193922291
PheGenIrs193922291
hapmaprs193922291
1000 genomesrs193922291
hgdprs193922291
ensemblrs193922291
gopubmedrs193922291
geneviewrs193922291
scholarrs193922291
googlers193922291
pharmgkbrs193922291
gwascentralrs193922291
openSNPrs193922291
23andMers193922291
23andMe allrs193922291
SNP Nexus

SNPshotrs193922291
SNPdbers193922291
MSV3drs193922291
GWAS Ctlgrs193922291
Max Magnitude0
ClinVar
Risk rs193922291(T;T)
Alt rs193922291(T;T)
Reference rs193922291(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.44191929T>A
CLNSRC ClinVar
CLNACC RCV000029874.1,