UGT1A6 c.861+35058A>G

Variant ID: 2-234637569-A-G

NM_001072.3(UGT1A6):c.861+35058A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


The Mutation Hotspots at UGT1A Locus May Be Associated with Gilbert's Syndrome Affecting the Taiwanese Population.

International Journal Of Molecular Sciences
Hsu, Paul Wei-Che PW; Liao, Po-Cheng PC; Kao, Yu-Hsiang YH; Lin, Xin-Yu XY; Chien, Rong-Nan RN; Yeh, Chau-Ting CT; Lai, Chi-Chun CC; Shyu, Yu-Chiau YC; Lin, Chih-Lang CL
Publication Date: 2022-10-21

Variant appearance in text: rs3806597
PubMed Link: 36293566
Variant Present in the following documents:
  • ijms-23-12709.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: rs3806597
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Comprehensive Pharmacogenomic Study Reveals an Important Role of UGT1A3 in Montelukast Pharmacokinetics.

Clinical Pharmacology And Therapeutics
Hirvensalo, Päivi P; Tornio, Aleksi A; Neuvonen, Mikko M; Tapaninen, Tuija T; Paile-Hyvärinen, Maria M; Kärjä, Vesa V; Männistö, Ville T VT; Pihlajamäki, Jussi J; Backman, Janne T JT; Niemi, Mikko M
Publication Date: 2018-07

Variant appearance in text: rs3806597
PubMed Link: 28940478
Variant Present in the following documents:
  • Main text
  • CPT-104-158.pdf
View BVdb publication page