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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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