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HTR2A c.614-6938T>C
Variant ID: 13-47416712-A-G
NM_000621.4(
HTR2A
):c.614-6938T>C
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Gene-Based Association Analysis Suggests Association of HTR2A With Antidepressant Treatment Response in Depressed Patients.
Frontiers In Pharmacology
Kao, Chung-Feng CF; Kuo, Po-Hsiu PH; Yu, Younger W-Y YW; Yang, Albert C AC; Lin, Eugene E; Liu, Yu-Li YL; Tsai, Shih-Jen SJ
Publication Date: 2020
Variant appearance in text: rs76703096
PubMed Link:
33519430
Variant Present in the following documents:
Main text
fphar-11-559601.pdf
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: rs76703096
PubMed Link:
30214008
Variant Present in the following documents:
NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page