GAA c.2041-1G>A

Variant ID: 17-78087016-G-A

NM_000152.3(GAA):c.2041-1G>A

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: GAA: 2041-1G>A; rs760731229
PubMed Link: 34078906
Variant Present in the following documents:
  • 41525_2021_203_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page