DRD2 c.285+1493A>C

Variant ID: 11-113293596-T-G

NM_000795.3(DRD2):c.285+1493A>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: rs2734831
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders.

Psychiatric Genetics
Stein, Catherine M CM; Truitt, Barbara B; Deng, Fenghua F; Ciesla, Allison Avrich AA; Qiu, Feiyou F; Joseph, Peronne P; Raghavendra, Rekha R; Fondran, Jeremy J; Igo, Robert P RP; Tag, Jessica J; Freebairn, Lisa L; Taylor, H Gerry HG; Lewis, Barbara A BA; Iyengar, Sudha K SK
Publication Date: 2014-10

Variant appearance in text: rs2734831
PubMed Link: 24849541
Variant Present in the following documents:
  • Main text
View BVdb publication page



A pilot study of genetic variants in dopamine regulators with indoor tanning and melanoma.

Experimental Dermatology
Flores, Kristina G KG; Erdei, Esther E; Luo, Li L; White, Kirsten A M KA; Leng, Shuguang S; Berwick, Marianne M; Lazovich, DeAnn D
Publication Date: 2013-09

Variant appearance in text: rs2734831
PubMed Link: 23947671
Variant Present in the following documents:
  • Main text
View BVdb publication page