Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2267386
rs2267386
Entrez Id: 3761;105373029
Gene Symbol: KCNJ4;LOC105373029
KCNJ4;LOC105373029
CUI: C1853238
Disease:
Conotruncal defect
0.700 GeneticVariation GWASDB Genome-wide association study of maternal and inherited loci for conotruncal heart defects. 24800985 2014