PCMTD1 c.410+1128C>T

Variant ID: 8-52757093-G-A

NM_052937.2(PCMTD1):c.410+1128C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Dataset of GWAS-identified variants underlying venous thromboembolism susceptibility and linkage to cancer aggressiveness.

Data In Brief
Tavares, Valéria V; Pinto, Ricardo R; Assis, Joana J; Pereira, Deolinda D; Medeiros, Rui R
Publication Date: 2020-06

Variant appearance in text: rs10504130
PubMed Link: 32258274
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.

Bmc Medical Genetics
Greliche, Nicolas N; Germain, Marine M; Lambert, Jean-Charles JC; Cohen, William W; Bertrand, Marion M; Dupuis, Anne-Marie AM; Letenneur, Luc L; Lathrop, Mark M; Amouyel, Philippe P; Morange, Pierre-Emmanuel PE; Trégouët, David-Alexandre DA
Publication Date: 2013-03-20

Variant appearance in text: rs10504130
PubMed Link: 23509962
Variant Present in the following documents:
  • Main text
  • 1471-2350-14-36.pdf
View BVdb publication page