SLCO1B1 c.970+739A>G

Variant ID: 12-21350861-A-G

NM_006446.4(SLCO1B1):c.970+739A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Single nucleotide polymorphisms associated with elevated alanine aminotransferase in patients receiving asunaprevir plus daclatasvir combination therapy for chronic hepatitis C.

Plos One
Kato, Keizo K; Shimada, Noritomo N; Atsukawa, Masanori M; Abe, Hiroshi H; Itokawa, Norio N; Matsumoto, Yoshihiro Y; Agata, Rie R; Tsubota, Akihito A
Publication Date: 2019

Variant appearance in text: rs4149064
PubMed Link: 31291311
Variant Present in the following documents:
  • Main text
  • pone.0219022.pdf
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs4149064
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page