rs1567941252, PCGF2

N. diseases: 10
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Abnormality of the outer ear
CUI: C1846460
Disease: Abnormality of the outer ear
0.700 GeneticVariation CLINVAR
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.700 GeneticVariation CLINVAR
Congenital Camptodactyly
CUI: C0685409
Disease: Congenital Camptodactyly
0.700 GeneticVariation CLINVAR
Low Vision
CUI: C0042798
Disease: Low Vision
0.700 GeneticVariation CLINVAR
Acid reflux
CUI: C4317146
Disease: Acid reflux
0.700 GeneticVariation CLINVAR
Poor school performance
CUI: C1843367
Disease: Poor school performance
0.700 GeneticVariation CLINVAR
Crumpled ear
CUI: C4024166
Disease: Crumpled ear
0.700 GeneticVariation CLINVAR
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
0.700 GeneticVariation CLINVAR
Constipation
CUI: C0009806
Disease: Constipation
0.700 GeneticVariation CLINVAR
Low set ears
CUI: C0239234
Disease: Low set ears
0.700 GeneticVariation CLINVAR