rs6545278, None

N. diseases: 2
Disease: Conotruncal defect ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Conotruncal defect
CUI: C1853238
Disease: Conotruncal defect
0.700 GeneticVariation GWASDB Genome-wide association study of maternal and inherited loci for conotruncal heart defects. 24800985 2014