SLC28A3 c.243-1776G>T

Variant ID: 9-86922036-C-A

NM_001199633.1(SLC28A3):c.243-1776G>T

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: rs10123041
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



High-density lipoprotein (HDL) cholesterol: leveraging practice-based biobank cohorts to characterize clinical and genetic predictors of treatment outcome.

The Pharmacogenomics Journal
Wilke, R A RA
Publication Date: 2011-06

Variant appearance in text: rs10123041
PubMed Link: 21151197
Variant Present in the following documents:
  • Main text
View BVdb publication page