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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.
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: 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