Bibliome.ai browser hg19
Search
About
Stats
FAQ
SLCO1B1 c.85-7319T>A
Variant ID: 12-21318265-T-A
NM_006446.4(
SLCO1B1
):c.85-7319T>A
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:
Implementation of Pharmacogenetics to Individualize Treatment Regimens for Children with Acute Lymphoblastic Leukemia.
Pharmacogenomics And Personalized Medicine
Maamari, Dimitri D; El-Khoury, Habib H; Saifi, Omran O; Muwakkit, Samar A SA; Zgheib, Nathalie K NK
Publication Date: 2020
Variant appearance in text: rs4149035
PubMed Link:
32848445
Variant Present in the following documents:
Main text
pgpm-13-295.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: rs4149035
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page