DRD2 c.285+113A>G

Variant ID: 11-113294976-T-C

NM_000795.3(DRD2):c.285+113A>G

This variant was identified in 9 publications

View GRCh38 version.




Publications:


A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: rs11608185
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
View BVdb publication page



Shared genetic liability between major depressive disorder and osteoarthritis.

Bone & Joint Research
Zhang, Fuquan F; Rao, Shuquan S; Baranova, Ancha A
Publication Date: 2022-01

Variant appearance in text: rs11608185
PubMed Link: 35023758
Variant Present in the following documents:
  • Main text
View BVdb publication page



DRD1 and DRD2 Receptor Polymorphisms: Genetic Neuromodulation of the Dopaminergic System as a Risk Factor for ASD, ADHD and ASD/ADHD Overlap.

Frontiers In Neuroscience
Mariggiò, Maria Addolorata MA; Palumbi, Roberto R; Vinella, Angela A; Laterza, Riccardo R; Petruzzelli, Maria Giuseppina MG; Peschechera, Antonia A; Gabellone, Alessandra A; Gentile, Ottavio O; Vincenti, Alessandra A; Margari, Lucia L
Publication Date: 2021

Variant appearance in text: rs11608185
PubMed Link: 34658761
Variant Present in the following documents:
  • Main text
  • fnins-15-705890.pdf
View BVdb publication page



Novel germline TRAF3IP3 mutation in a dyad with familial acute B lymphoblastic leukemia.

Cancer Reports (Hoboken, N.J.)
Pommert, Lauren L; Burns, Robert R; Furumo, Quinlan Q; Pulakanti, Kirthi K; Brandt, Jon J; Burke, Michael J MJ; Rao, Sridhar S
Publication Date: 2021-06

Variant appearance in text: DRD2: 285+113A>G; rs11608185
PubMed Link: 33503336
Variant Present in the following documents:
  • CNR2-4-e1335-s003.xlsx, sheet 1
  • CNR2-4-e1335-s003.xlsx, sheet 2
View BVdb publication page



Systematic Review and Meta-Analysis of Genetic Risk of Developing Chronic Postsurgical Pain.

The Journal Of Pain
Chidambaran, Vidya V; Gang, Yang Y; Pilipenko, Valentina V; Ashton, Maria M; Ding, Lili L
Publication Date: 2020

Variant appearance in text: rs11608185
PubMed Link: 31129315
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs11608185
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Genetics of schizophrenia from a clinicial perspective.

International Review Of Psychiatry (Abingdon, England)
Kukshal, Prachi P; Thelma, B K BK; Nimgaonkar, Vishwajit L VL; Deshpande, Smita N SN
Publication Date: 2012-10

Variant appearance in text: rs11608185
PubMed Link: 23057976
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genomics and pharmacogenomics of schizophrenia.

Cns Neuroscience & Therapeutics
Cacabelos, Ramón R; Martínez-Bouza, Rocío R
Publication Date: 2011-10

Variant appearance in text: rs11608185
PubMed Link: 20718829
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.

Molecular Pain
Kim, Hyungsuk H; Lee, Hyewon H; Rowan, Janet J; Brahim, Jaime J; Dionne, Raymond A RA
Publication Date: 2006-07-18

Variant appearance in text: rs11608185
PubMed Link: 16848906
Variant Present in the following documents:
  • Main text
  • 1744-8069-2-24.pdf
View BVdb publication page