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DRD2 c.-31-9053C>T
Variant ID: 11-113304457-G-A
NM_000795.3(
DRD2
):c.-31-9053C>T
This variant was identified in 4 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: rs7122246
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
The Association of DRD2 with Insight Problem Solving.
Frontiers In Psychology
Zhang, Shun S; Zhang, Jinghuan J
Publication Date: 2016
Variant appearance in text: rs7122246
PubMed Link:
27933030
Variant Present in the following documents:
Main text
fpsyg-07-01865.pdf
View BVdb publication page
Clinical and genetic factors related to cancer-induced bone pain and bone pain relief.
The Oncologist
Scarpi, Emanuela E; Calistri, Daniele D; Klepstad, Pål P; Kaasa, Stein S; Skorpen, Frank F; Habberstad, Ragnhild R; Nanni, Oriana O; Amadori, Dino D; Maltoni, Marco M
Publication Date: 2014-12
Variant appearance in text: rs7122246
PubMed Link:
25342315
Variant Present in the following documents:
Main text
View BVdb publication page
Gender-stratified gene and gene-treatment interactions in smoking cessation.
The Pharmacogenomics Journal
Lee, W W; Bergen, A W AW; Swan, G E GE; Li, D D; Liu, J J; Thomas, P P; Tyndale, R F RF; Benowitz, N L NL; Lerman, C C; Conti, D V DV
Publication Date: 2012-12
Variant appearance in text: rs7122246
PubMed Link:
21808284
Variant Present in the following documents:
NIHMS305090-supplement-3.pdf
View BVdb publication page