XRCC5 c.1834+4557T>C

Variant ID: 2-217031328-T-C

NM_021141.3(XRCC5):c.1834+4557T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Non-homologous end-joining pathway associated with occurrence of myocardial infarction: gene set analysis of genome-wide association study data.

Plos One
Verschuren, Jeffrey J W JJ; Trompet, Stella S; Deelen, Joris J; Stott, David J DJ; Sattar, Naveed N; Buckley, Brendan M BM; Ford, Ian I; Heijmans, Bastiaan T BT; Guchelaar, Henk-Jan HJ; Houwing-Duistermaat, Jeanine J JJ; Slagboom, P Eline PE; Jukema, J Wouter JW
Publication Date: 2013

Variant appearance in text: rs3821107
PubMed Link: 23457540
Variant Present in the following documents:
  • Main text
  • pone.0056262.pdf
View BVdb publication page



Associations between single nucleotide polymorphisms in double-stranded DNA repair pathway genes and familial breast cancer.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Sehl, Mary E ME; Langer, Lucy R LR; Papp, Jeanette C JC; Kwan, Lorna L; Seldon, Joyce L JL; Arellano, Geovanni G; Reiss, Jean J; Reed, Elaine F EF; Dandekar, Sugandha S; Korin, Yael Y; Sinsheimer, Janet S JS; Zhang, Zuo-Feng ZF; Ganz, Patricia A PA
Publication Date: 2009-03-15

Variant appearance in text: rs3821107
PubMed Link: 19276285
Variant Present in the following documents:
  • Main text
View BVdb publication page