LPA c.49+2351C>T

Variant ID: 6-161082847-G-A

NM_005577.2(LPA):c.49+2351C>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: rs1367209
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk.

Stroke
Ronald, James J; Rajagopalan, Ramakrishnan R; Cerrato, Felecia F; Nord, Alex S AS; Hatsukami, Thomas T; Kohler, Ted T; Marcovina, Santica S; Heagerty, Patrick P; Jarvik, Gail P GP
Publication Date: 2011-01

Variant appearance in text: rs1367209
PubMed Link: 21127300
Variant Present in the following documents:
  • Main text
View BVdb publication page