Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3924389
rs3924389
Entrez Id: 158293
Gene Symbol: FAM120AOS
FAM120AOS
CUI: C0596887
Disease:
mathematical ability 		G 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
dbSNP: rs140119177
rs140119177
Entrez Id: 158293
Gene Symbol: FAM120AOS
FAM120AOS
CUI: C0016842
Disease:
Congenital pectus excavatum 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs140119177
rs140119177
Entrez Id: 158293
Gene Symbol: FAM120AOS
FAM120AOS
CUI: C0746102
Disease:
Chronic lung disease 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs140119177
rs140119177
Entrez Id: 158293
Gene Symbol: FAM120AOS
FAM120AOS
CUI: C0036439
Disease:
Scoliosis, unspecified 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs140119177
rs140119177
Entrez Id: 158293
Gene Symbol: FAM120AOS
FAM120AOS
CUI: C0026827
Disease:
Muscle hypotonia 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs140119177
rs140119177
Entrez Id: 158293
Gene Symbol: FAM120AOS
FAM120AOS
CUI: C1845847
Disease:
Coarse facial features 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs140119177
rs140119177
Entrez Id: 158293
Gene Symbol: FAM120AOS
FAM120AOS
CUI: C0010495
Disease:
Cutis Laxa 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs140119177
rs140119177
Entrez Id: 158293
Gene Symbol: FAM120AOS
FAM120AOS
CUI: C4317146
Disease:
Acid reflux 		A 0.700 GeneticVariation CLINVAR