rs870142, STX18-AS1

N. diseases: 7
Disease: Congenital heart disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
0.710 GeneticVariation BEFREE A recent European genome-wide association study (GWAS) of congenital heart disease (CHD) identified 3 susceptibility SNPs at chromosome 4p16 associated with ASD: rs870142, rs16835979 and rs6824295. 25875170 2015
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
0.710 GeneticVariation GWASDB Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. 23708191 2013