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rs1719247

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1719247(C;T)
Make rs1719247(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position45328787
is asnp
is mentioned by
dbSNPrs1719247
ebirs1719247
HLIrs1719247
Exacrs1719247
Varsomers1719247
Maprs1719247
PheGenIrs1719247
hapmaprs1719247
1000 genomesrs1719247
hgdprs1719247
ensemblrs1719247
gopubmedrs1719247
geneviewrs1719247
scholarrs1719247
googlers1719247
pharmgkbrs1719247
gwascentralrs1719247
openSNPrs1719247
23andMers1719247
23andMe allrs1719247
SNP Nexus

SNPshotrs1719247
SNPdbers1719247
MSV3drs1719247
GWAS Ctlgrs1719247
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs1719247(T;T)
Alt rs1719247(T;T)
Reference rs1719247(C;C)
Significance Drug-response
Disease hmg coa reductase inhibitors response - Toxicity/ADR simvastatin response - Toxicity/ADR
Variation info
Gene
CLNDBN hmg coa reductase inhibitors response - Toxicity/ADR simvastatin response - Toxicity/ADR
Reversed 0
HGVS NC_000015.9:g.45620985C>T
CLNSRC PharmGKB Clinical Annotation PharmGKB
CLNACC RCV000211134.1, RCV000211259.1,