SFMBT1 c.123+688A>C

Variant ID: 3-52987645-T-G

NM_016329.3(SFMBT1):c.123+688A>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.

Medrxiv : The Preprint Server For Health Sciences
Tadros, Rafik R; Zheng, Sean L SL; Grace, Christopher C; Jordà, Paloma P; Francis, Catherine C; Jurgens, Sean J SJ; Thomson, Kate L KL; Harper, Andrew R AR; Ormondroyd, Elizabeth E; West, Dominique M DM; Xu, Xiao X; Theotokis, Pantazis I PI; Buchan, Rachel J RJ; McGurk, Kathryn A KA; Mazzarotto, Francesco F; Boschi, Beatrice B; Pelo, Elisabetta E; Lee, Michael M; Noseda, Michela M; Varnava, Amanda A; Vermeer, Alexa Mc AM; Walsh, Roddy R; Amin, Ahmad S AS; van Slegtenhorst, Marjon A MA; Roslin, Nicole N; Strug, Lisa J LJ; Salvi, Erika E; Lanzani, Chiara C; de Marvao, Antonio A; , ; Roberts, Jason D JD; Tremblay-Gravel, Maxime M; Giraldeau, Genevieve G; Cadrin-Tourigny, Julia J; L'Allier, Philippe L PL; Garceau, Patrick P; Talajic, Mario M; Pinto, Yigal M YM; Rakowski, Harry H; Pantazis, Antonis A; Baksi, John J; Halliday, Brian P BP; Prasad, Sanjay K SK; Barton, Paul Jr PJ; O'Regan, Declan P DP; Cook, Stuart A SA; de Boer, Rudolf A RA; Christiaans, Imke I; Michels, Michelle M; Kramer, Christopher M CM; Ho, Carolyn Y CY; Neubauer, Stefan S; , ; Matthews, Paul M PM; Wilde, Arthur A AA; Tardif, Jean-Claude JC; Olivotto, Iacopo I; Adler, Arnon A; Goel, Anuj A; Ware, James S JS; Bezzina, Connie R CR; Watkins, Hugh H
Publication Date: 2023-02-06

Variant appearance in text: rs9311485
PubMed Link: 36778260
Variant Present in the following documents:
  • nihpp-2023.01.28.23285147v2.pdf
View BVdb publication page