UGT1A1 c.997-37T>C

Variant ID: 2-234676458-T-C

NM_000463.2(UGT1A1):c.997-37T>C

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Common UGT1A9 polymorphisms do not have a clinically meaningful impact on the apparent oral clearance of dapagliflozin in type 2 diabetes mellitus.

British Journal Of Clinical Pharmacology
Naagaard, M Daniel MD; Chang, Roy R; Någård, Mats M; Tang, Weifeng W; Boulton, David W DW
Publication Date: 2022-02

Variant appearance in text: rs12471326
PubMed Link: 34687551
Variant Present in the following documents:
  • BCP-88-1942-s001.xlsx, sheet 5
View BVdb publication page



Genetic variants in CYP2A6 and UGT1A9 genes associated with urinary nicotine metabolites in young Mexican smokers.

The Pharmacogenomics Journal
Borrego-Soto, Gissela G; Perez-Paramo, Yadira X YX; Chen, Gang G; Santuario-Facio, Sandra K SK; Santos-Guzman, Jesus J; Posadas-Valay, Rodolfo R; Alvarado-Monroy, Fatima M FM; Balderas-Renteria, Isaias I; Medina-Gonzalez, Ramses R; Ortiz-Lopez, Rocio R; Lazarus, Philip P; Rojas-Martinez, Augusto A
Publication Date: 2020-08

Variant appearance in text: rs12471326
PubMed Link: 31959879
Variant Present in the following documents:
  • Main text
  • 41397_2020_Article_147.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: rs12471326
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Sporadic hemangioblastomas are characterized by cryptic VHL inactivation.

Acta Neuropathologica Communications
Shankar, Ganesh M GM; Taylor-Weiner, Amaro A; Lelic, Nina N; Jones, Robert T RT; Kim, James C JC; Francis, Joshua M JM; Abedalthagafi, Malak M; Borges, Lawrence F LF; Coumans, Jean-Valery JV; Curry, William T WT; Nahed, Brian V BV; Shin, John H JH; Paek, Sun Ha SH; Park, Sung-Hye SH; Stewart, Chip C; Lawrence, Michael S MS; Cibulskis, Kristian K; Thorner, Aaron R AR; Van Hummelen, Paul P; Stemmer-Rachamimov, Anat O AO; Batchelor, Tracy T TT; Carter, Scott L SL; Hoang, Mai P MP; Santagata, Sandro S; Louis, David N DN; Barker, Fred G FG; Meyerson, Matthew M; Getz, Gad G; Brastianos, Priscilla K PK; Cahill, Daniel P DP
Publication Date: 2014-12-24

Variant appearance in text: rs12471326
PubMed Link: 25589003
Variant Present in the following documents:
  • 40478_2014_167_MOESM1_ESM.xlsx, sheet 6
View BVdb publication page



Comprehensive variant screening of the UGT gene family.

Yonsei Medical Journal
Kim, Jason Yongha JY; Cheong, Hyun Sub HS; Park, Byung Lae BL; Kim, Lyoung Hyo LH; Namgoong, Suhg S; Kim, Ji On JO; Kim, Hae Deun HD; Kim, Young Hoon YH; Chung, Myeon Woo MW; Han, Soon Young SY; Shin, Hyoung Doo HD
Publication Date: 2014-01

Variant appearance in text: rs12471326
PubMed Link: 24339312
Variant Present in the following documents:
  • ymj-55-232.pdf
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: rs12471326
PubMed Link: 21513526
Variant Present in the following documents:
  • Main text
  • 1471-2350-12-57.pdf
View BVdb publication page