DRD2 c.-31-703T>C

Variant ID: 11-113296107-A-G

NM_000795.3(DRD2):c.-31-703T>C

This variant was identified in 3 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: rs1116313
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Dopamine receptors and BDNF-haplotypes predict dyskinesia in Parkinson's disease.

Parkinsonism & Related Disorders
Kusters, Cynthia D J CDJ; Paul, Kimberly C KC; Guella, Ilaria I; Bronstein, Jeff M JM; Sinsheimer, Janet S JS; Farrer, Matt J MJ; Ritz, Beate R BR
Publication Date: 2018-02

Variant appearance in text: rs1116313
PubMed Link: 29191473
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic influences on craving for alcohol.

Addictive Behaviors
Agrawal, Arpana A; Wetherill, Leah L; Bucholz, Kathleen K KK; Kramer, John J; Kuperman, Samuel S; Lynskey, Michael T MT; Nurnberger, John I JI; Schuckit, Marc M; Tischfield, Jay A JA; Edenberg, Howard J HJ; Foroud, Tatiana T; Bierut, Laura J LJ
Publication Date: 2013-02

Variant appearance in text: rs1116313
PubMed Link: 22481050
Variant Present in the following documents:
  • Main text
View BVdb publication page