Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607106
rs267607106
TBX20
0.800 GeneticVariation UNIPROT A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects. 19762328

2010
dbSNP: rs267607106
rs267607106
TBX20
0.800 GeneticVariation UNIPROT Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy. 17668378

2007
dbSNP: rs267607106
rs267607106
TBX20
C 0.800 CausalMutation CLINVAR