USP1 c.170+185C>T

Variant ID: 1-62905893-C-T

NM_003368.4(USP1):c.170+185C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


A phenome-wide association study (PheWAS) in the Population Architecture using Genomics and Epidemiology (PAGE) study reveals potential pleiotropy in African Americans.

Plos One
Pendergrass, Sarah A SA; Buyske, Steven S; Jeff, Janina M JM; Frase, Alex A; Dudek, Scott S; Bradford, Yuki Y; Ambite, Jose-Luis JL; Avery, Christy L CL; Buzkova, Petra P; Deelman, Ewa E; Fesinmeyer, Megan D MD; Haiman, Christopher C; Heiss, Gerardo G; Hindorff, Lucia A LA; Hsu, Chun-Nan CN; Jackson, Rebecca D RD; Lin, Yi Y; Le Marchand, Loic L; Matise, Tara C TC; Monroe, Kristine R KR; Moreland, Larry L; North, Kari E KE; Park, Sungshim L SL; Reiner, Alex A; Wallace, Robert R; Wilkens, Lynne R LR; Kooperberg, Charles C; Ritchie, Marylyn D MD; Crawford, Dana C DC
Publication Date: 2019

Variant appearance in text: rs10493322
PubMed Link: 31891604
Variant Present in the following documents:
  • Main text
  • pone.0226771.pdf
View BVdb publication page



Low LDL cholesterol, PCSK9 and HMGCR genetic variation, and risk of Alzheimer's disease and Parkinson's disease: Mendelian randomisation study.

Bmj (Clinical Research Ed.)
Benn, Marianne M; Nordestgaard, Børge G BG; Frikke-Schmidt, Ruth R; Tybjærg-Hansen, Anne A
Publication Date: 2017-04-24

Variant appearance in text: rs10493322
PubMed Link: 28438747
Variant Present in the following documents:
  • benm033277.ww1.pdf
View BVdb publication page



Post-GWAS methodologies for localisation of functional non-coding variants: ANGPTL3.

Atherosclerosis
Oldoni, Federico F; Palmen, Jutta J; Giambartolomei, Claudia C; Howard, Philip P; Drenos, Fotios F; Plagnol, Vincent V; Humphries, Steve E SE; Talmud, Philippa J PJ; Smith, Andrew J P AJ
Publication Date: 2016-03

Variant appearance in text: rs10493322
PubMed Link: 26800306
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page