The original data of the whole exome sequencing for eighteen Tibetan PFO patients

Patent foramen ovale (PFO), a prevalent congenital cardiac defectanomaly, is linked to clinical conditions such as cryptogenic stroke and migraine. The genetic underpinnings of PFO remain poorly elucidated, particularly in Tibet. This study aimed to identify potential pathogenic mutations in Tibetan PFO patients via whole-exome sequencing (WES) to clarify its genetic basis.This study employs WES technology to investigate genetic characteristics of PFO in Tibetan populations, focusing on identifying disease-associated mutations.