UGT1A6 c.862-10182C>T

Variant ID: 2-234665498-C-T

NM_001072.3(UGT1A6):c.862-10182C>T

This variant was identified in 5 publications

View GRCh38 version.




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: rs11568318
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



PheWAS and Beyond: The Landscape of Associations with Medical Diagnoses and Clinical Measures across 38,662 Individuals from Geisinger.

American Journal Of Human Genetics
Verma, Anurag A; Lucas, Anastasia A; Verma, Shefali S SS; Zhang, Yu Y; Josyula, Navya N; Khan, Anqa A; Hartzel, Dustin N DN; Lavage, Daniel R DR; Leader, Joseph J; Ritchie, Marylyn D MD; Pendergrass, Sarah A SA
Publication Date: 2018-04-05

Variant appearance in text: rs11568318
PubMed Link: 29606303
Variant Present in the following documents:
  • Main text
View BVdb publication page



Characterization of ADME gene variation in 21 populations by exome sequencing.

Pharmacogenetics And Genomics
Hovelson, Daniel H DH; Xue, Zhengyu Z; Zawistowski, Matthew M; Ehm, Margaret G MG; Harris, Elizabeth C EC; Stocker, Sophie L SL; Gross, Annette S AS; Jang, In-Jin IJ; Ieiri, Ichiro I; Lee, Jong-Eun JE; Cardon, Lon R LR; Chissoe, Stephanie L SL; Abecasis, Gonçalo G; Nelson, Matthew R MR
Publication Date: 2017-03

Variant appearance in text: rs11568318
PubMed Link: 27984508
Variant Present in the following documents:
  • fpc-27-089-s005.xlsx, sheet 2
View BVdb publication page



Novel genomic signals of recent selection in an Ethiopian population.

European Journal Of Human Genetics : Ejhg
Tekola-Ayele, Fasil F; Adeyemo, Adebowale A; Chen, Guanjie G; Hailu, Elena E; Aseffa, Abraham A; Davey, Gail G; Newport, Melanie J MJ; Rotimi, Charles N CN
Publication Date: 2015-08

Variant appearance in text: rs11568318
PubMed Link: 25370040
Variant Present in the following documents:
  • Main text
View BVdb publication page



UGT1A1 sequence variants and bilirubin levels in early postnatal life: a quantitative approach.

Bmc Medical Genetics
Hanchard, Neil A NA; Skierka, Jennifer J; Weaver, Amy A; Karon, Brad S BS; Matern, Dietrich D; Cook, Walter W; O'Kane, Dennis J DJ
Publication Date: 2011-04-22

Variant appearance in text: rs11568318
PubMed Link: 21513526
Variant Present in the following documents:
  • Main text
  • 1471-2350-12-57.pdf
View BVdb publication page