KCNQ1 c.1129-2A>G

Variant ID: 11-2608798-A-G

NM_000218.2(KCNQ1):c.1129-2A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The prevalence, genetic complexity and population-specific founder effects of human autosomal recessive disorders.

Npj Genomic Medicine
Xiao, Qingyang Q; Lauschke, Volker M VM
Publication Date: 2021-06-02

Variant appearance in text: KCNQ1: 1129-2A>G; rs768022350
PubMed Link: 34078906
Variant Present in the following documents:
  • 41525_2021_203_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page