APOA1, apolipoprotein A1, 335

N. diseases: 416; N. variants: 32
Disease: Pyloric Stenosis, Hypertrophic ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12721025
rs12721025
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0700639
Disease:
Pyloric Stenosis, Hypertrophic 		A 0.800 GeneticVariation GWASCAT Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis. 30281099 2019
dbSNP: rs12721025
rs12721025
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0700639
Disease:
Pyloric Stenosis, Hypertrophic 		A 0.800 GeneticVariation GWASDB Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis. 23989729 2013
dbSNP: rs12721025
rs12721025
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0700639
Disease:
Pyloric Stenosis, Hypertrophic 		A 0.800 GeneticVariation GWASCAT Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis. 23989729 2013