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rs193922315

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922315(C;C)
Make rs193922315(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44149781
GeneGCK
is asnp
is mentioned by
dbSNPrs193922315
ebirs193922315
HLIrs193922315
Exacrs193922315
Varsomers193922315
Maprs193922315
PheGenIrs193922315
hapmaprs193922315
1000 genomesrs193922315
hgdprs193922315
ensemblrs193922315
gopubmedrs193922315
geneviewrs193922315
scholarrs193922315
googlers193922315
pharmgkbrs193922315
gwascentralrs193922315
openSNPrs193922315
23andMers193922315
23andMe allrs193922315
SNP Nexus

SNPshotrs193922315
SNPdbers193922315
MSV3drs193922315
GWAS Ctlgrs193922315
Max Magnitude0
ClinVar
Risk rs193922315(C;C)
Alt rs193922315(C;C)
Reference rs193922315(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.44189380A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029902.1,