SLCO1B1 c.85-10169A>C

Variant ID: 12-21315415-A-C

NM_006446.4(SLCO1B1):c.85-10169A>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Ensemble learning for the early prediction of neonatal jaundice with genetic features.

Bmc Medical Informatics And Decision Making
Deng, Haowen H; Zhou, Youyou Y; Wang, Lin L; Zhang, Cheng C
Publication Date: 2021-12-01

Variant appearance in text: rs4149026
PubMed Link: 34852805
Variant Present in the following documents:
  • Main text
  • 12911_2021_Article_1701.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: rs4149026
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page