SLC22A1 c.839+886C>G

Variant ID: 6-160556043-C-G

NM_003057.2(SLC22A1):c.839+886C>G

This variant was identified in 3 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: rs3798172
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Metabolic heritability at birth: implications for chronic disease research.

Human Genetics
Ryckman, Kelli K KK; Smith, Caitlin J CJ; Jelliffe-Pawlowski, Laura L LL; Momany, Allison M AM; Berberich, Stanton L SL; Murray, Jeffrey C JC
Publication Date: 2014-08

Variant appearance in text: rs3798172
PubMed Link: 24850141
Variant Present in the following documents:
  • Main text
View BVdb publication page



SLC22A1-ABCB1 haplotype profiles predict imatinib pharmacokinetics in Asian patients with chronic myeloid leukemia.

Plos One
Singh, Onkar O; Chan, Jason Yongsheng JY; Lin, Keegan K; Heng, Charles Chuah Thuan CC; Chowbay, Balram B
Publication Date: 2012

Variant appearance in text: rs3798172
PubMed Link: 23272163
Variant Present in the following documents:
  • Main text
  • pone.0051771.pdf
View BVdb publication page