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DRD2 c.-31-7110G>T
Variant ID: 11-113302514-C-A
NM_000795.3(
DRD2
):c.-31-7110G>T
This variant was identified in 3 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: rs12800853
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page
Selection in the dopamine receptor 2 gene: a candidate SNP study.
Peerj
Göllner, Tobias T; Fieder, Martin M
Publication Date: 2015
Variant appearance in text: rs12800853
PubMed Link:
26290802
Variant Present in the following documents:
Main text
peerj-03-1149.pdf
View BVdb publication page
Stuttering candidate genes DRD2 but not SLC6A3 is associated with developmental dyslexia in Chinese population.
Behavioral And Brain Functions : Bbf
Chen, Huan H; Wang, Guoqing G; Xia, Jiguang J; Zhou, Yuxi Y; Gao, Yong Y; Xu, Junquan J; Huen, Michael Sy MS; Siok, Wai Ting WT; Jiang, Yuyang Y; Tan, Li Hai LH; Sun, Yimin Y
Publication Date: 2014-09-01
Variant appearance in text: rs12800853
PubMed Link:
25178928
Variant Present in the following documents:
Main text
1744-9081-10-29.pdf
View BVdb publication page