Gene: TBX5 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555223259
rs1555223259
TBX5
C 0.700 CausalMutation CLINVAR A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data. 29555671

2018
dbSNP: rs1555226315
rs1555226315
TBX5
T 0.700 CausalMutation CLINVAR

dbSNP: rs11067075
rs11067075
TBX5
0.010 GeneticVariation BEFREE SNP rs11067075 within the TBX5 gene had significant correlation with ventricular septal defect (P = 0.0037) by single marker association analysis. 19187613

2009