SLCO1B1 c.1683-396A>G

Variant ID: 12-21374838-A-G

NM_006446.4(SLCO1B1):c.1683-396A>G

This variant was identified in 2 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: rs987839
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS).

Neurobiology Of Aging
Shi, Hui H; Belbin, Olivia O; Medway, Christopher C; Brown, Kristelle K; Kalsheker, Noor N; Carrasquillo, Minerva M; Proitsi, Petroula P; Powell, John J; Lovestone, Simon S; Goate, Alison A; Younkin, Steven S; Passmore, Peter P; , ; Morgan, Kevin K; ,
Publication Date: 2012-08

Variant appearance in text: rs987839
PubMed Link: 22445811
Variant Present in the following documents:
  • Main text
View BVdb publication page