LPA c.210-765T>C

Variant ID: 6-161068192-A-G

NM_005577.2(LPA):c.210-765T>C

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: rs78822335
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

Nature Communications
Zekavat, Seyedeh M SM; Ruotsalainen, Sanni S; Handsaker, Robert E RE; Alver, Maris M; Bloom, Jonathan J; Poterba, Timothy T; Seed, Cotton C; Ernst, Jason J; Chaffin, Mark M; Engreitz, Jesse J; Peloso, Gina M GM; Manichaikul, Ani A; Yang, Chaojie C; Ryan, Kathleen A KA; Fu, Mao M; Johnson, W Craig WC; Tsai, Michael M; Budoff, Matthew M; Vasan, Ramachandran S RS; Cupples, L Adrienne LA; Rotter, Jerome I JI; Rich, Stephen S SS; Post, Wendy W; Mitchell, Braxton D BD; Correa, Adolfo A; Metspalu, Andres A; Wilson, James G JG; Salomaa, Veikko V; Kellis, Manolis M; Daly, Mark J MJ; Neale, Benjamin M BM; McCarroll, Steven S; Surakka, Ida I; Esko, Tonu T; Ganna, Andrea A; Ripatti, Samuli S; Kathiresan, Sekar S; Natarajan, Pradeep P; ,
Publication Date: 2018-07-04

Variant appearance in text: rs78822335
PubMed Link: 29973585
Variant Present in the following documents:
  • 41467_2018_Article_4668.pdf
View BVdb publication page