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
dbSNP: rs2267386
rs2267386
Entrez Id: 3761;105373029
Gene Symbol: KCNJ4;LOC105373029
KCNJ4;LOC105373029
CUI: C1857586
Disease:
CONOTRUNCAL HEART MALFORMATIONS (disorder)
0.700 GeneticVariation GWASCAT Genome-wide association study of maternal and inherited loci for conotruncal heart defects. 24800985 2014
dbSNP: rs11704277
rs11704277
Entrez Id: 3761;101927183
Gene Symbol: KCNJ4;LOC101927183
KCNJ4;LOC101927183
CUI: C0596887
Disease:
mathematical ability
C 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018