rs140119177, FAM120AOS

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital pectus excavatum
CUI: C0016842
Disease: Congenital pectus excavatum
0.700 GeneticVariation CLINVAR
Chronic lung disease
CUI: C0746102
Disease: Chronic lung disease
0.700 GeneticVariation CLINVAR
Scoliosis, unspecified
CUI: C0036439
Disease: Scoliosis, unspecified
0.700 GeneticVariation CLINVAR
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
0.700 GeneticVariation CLINVAR
Coarse facial features
CUI: C1845847
Disease: Coarse facial features
0.700 GeneticVariation CLINVAR
Cutis Laxa
CUI: C0010495
Disease: Cutis Laxa
0.700 GeneticVariation CLINVAR
Acid reflux
CUI: C4317146
Disease: Acid reflux
0.700 GeneticVariation CLINVAR