rs1383180, CRMP1;EVC

N. diseases: 1
Disease: Ventricular Septal Defects ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
0.010 GeneticVariation BEFREE The c.1727G>A SNP of the EVC gene increased VSD susceptibility in patients from the Chinese Han population. 29257216 2018