KCNQ1 c.604+12C>T

Variant ID: 11-2591996-C-T

NM_000218.2(KCNQ1):c.604+12C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


KCNQ1 and Long QT Syndrome in 1/45 Amish: The Road From Identification to Implementation of Culturally Appropriate Precision Medicine.

Circulation. Genomic And Precision Medicine
Streeten, Elizabeth A EA; See, Vincent Y VY; Jeng, Linda B J LBJ; Maloney, Kristin A KA; Lynch, Megan M; Glazer, Andrew M AM; Yang, Tao T; Roden, Dan D; Pollin, Toni I TI; Daue, Melanie M; Ryan, Kathleen A KA; Van Hout, Cristopher C; Gosalia, Nehal N; Gonzaga-Jauregui, Claudia C; Economides, Aris A; Perry, James A JA; O'Connell, Jeffrey J; Beitelshees, Amber A; Palmer, Kathleen K; Mitchell, Braxton D BD; Shuldiner, Alan R AR; ,
Publication Date: 2020-12

Variant appearance in text: KCNQ1: 604+12C>T; rs370821907
PubMed Link: 33141630
Variant Present in the following documents:
  • hcg-13-e003133-s002.xls, sheet 1
View BVdb publication page