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rs1346268

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1346268(C;C)
Make rs1346268(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position45380831
GeneGATM
is asnp
is mentioned by
dbSNPrs1346268
ebirs1346268
HLIrs1346268
Exacrs1346268
Varsomers1346268
Maprs1346268
PheGenIrs1346268
hapmaprs1346268
1000 genomesrs1346268
hgdprs1346268
ensemblrs1346268
gopubmedrs1346268
geneviewrs1346268
scholarrs1346268
googlers1346268
pharmgkbrs1346268
gwascentralrs1346268
openSNPrs1346268
23andMers1346268
23andMe allrs1346268
SNP Nexus

SNPshotrs1346268
SNPdbers1346268
MSV3drs1346268
GWAS Ctlgrs1346268
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs1346268(C;C)
Alt rs1346268(C;C)
Reference rs1346268(T;T)
Significance Drug-response
Disease simvastatin response - Toxicity/ADR hmg coa reductase inhibitors response - Toxicity/ADR
Variation info
Gene
CLNDBN simvastatin response - Toxicity/ADR hmg coa reductase inhibitors response - Toxicity/ADR
Reversed 0
HGVS NC_000015.9:g.45673029T>C
CLNSRC PharmGKB Clinical Annotation PharmGKB
CLNACC RCV000211216.1, RCV000211394.1,