SLCO1B1 c.970+274T>C

Variant ID: 12-21350396-T-C

NM_006446.4(SLCO1B1):c.970+274T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: rs7957274
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



DNA-mediated dimerization on a compact sequence signature controls enhancer engagement and regulation by FOXA1.

Nucleic Acids Research
Wang, Xuecong X; Srivastava, Yogesh Y; Jankowski, Aleksander A; Malik, Vikas V; Wei, Yuanjie Y; Del Rosario, Ricardo Ch RC; Cojocaru, Vlad V; Prabhakar, Shyam S; Jauch, Ralf R
Publication Date: 2018-06-20

Variant appearance in text: rs7957274
PubMed Link: 29669022
Variant Present in the following documents:
  • Main text
  • gky259.pdf
  • gky259_supplemental_files.pdf
View BVdb publication page