PLPP3 c.810+3557C>T

Variant ID: 1-56974091-G-A

NM_003713.4(PLPP3):c.810+3557C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs1319274
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



Genetic Susceptibility Loci for Cardiovascular Disease and Their Impact on Atherosclerotic Plaques.

Circulation. Genomic And Precision Medicine
van der Laan, Sander W SW; Siemelink, Marten A MA; Haitjema, Saskia S; Foroughi Asl, Hassan H; Perisic, Ljubica L; Mokry, Michal M; van Setten, Jessica J; Malik, Rainer R; Dichgans, Martin M; Worrall, Bradford B BB; , ; Samani, Nilesh J NJ; Schunkert, Heribert H; Erdmann, Jeanette J; Hedin, Ulf U; Paulsson-Berne, Gabrielle G; Björkegrenn, Johan L M JLM; de Borst, Gert J GJ; Asselbergs, Folkert W FW; den Ruijter, Folkert W FW; de Bakker, Paul I W PIW; Pasterkamp, Gerard G
Publication Date: 2018-09

Variant appearance in text: rs1319274
PubMed Link: 30354329
Variant Present in the following documents:
  • hcg-11-e002115-s001.pdf
View BVdb publication page