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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.
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: 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