LPA c.3948-983G>T

Variant ID: 6-161008645-C-A

NM_005577.2(LPA):c.3948-983G>T

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: rs4073498
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Variation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination Survey.

Plos One
Dumitrescu, Logan L; Glenn, Kimberly K; Brown-Gentry, Kristin K; Shephard, Cynthia C; Wong, Michelle M; Rieder, Mark J MJ; Smith, Joshua D JD; Nickerson, Deborah A DA; Crawford, Dana C DC
Publication Date: 2011-01-28

Variant appearance in text: rs4073498
PubMed Link: 21305047
Variant Present in the following documents:
  • Main text
  • pone.0016604.pdf
View BVdb publication page