Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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