KCNQ1 c.160_161insATCGCGCCC ;(p.I54delinsNRAL)

Variant ID: 11-2466488-A-AATCGCGCCC

NM_000218.2(KCNQ1):c.160_161insATCGCGCCC;(p.I54delinsNRAL)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Atrial fibrillation: the role of common and rare genetic variants.

European Journal Of Human Genetics : Ejhg
Olesen, Morten S MS; Nielsen, Morten W MW; Haunsø, Stig S; Svendsen, Jesper H JH
Publication Date: 2014-03

Variant appearance in text: KCNQ1: 160_168insATCGCGCCC
PubMed Link: 23838598
Variant Present in the following documents:
  • Main text
View BVdb publication page