rs2231142, ABCG2

N. diseases: 56
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Heart Septal Defects
CUI: C0018816
Disease: Heart Septal Defects
0.010 GeneticVariation BEFREE This study aimed at exploring the associations between 421C>A and 34G>A polymorphisms within the ABCG2 gene of the children and isolated septal defects in a Han Chinese population. 24979295 2014