Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Attention deficit hyperactivity disorder
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
420 0.807 0.280 15 89326678 frameshift variant A/- delins 0.700 1.000 3 2010 2017
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.807 0.280 15 89326678 frameshift variant A/- delins 0.700 1.000 3 2010 2017
Constipation
CUI: C0009806
Disease: Constipation
57 0.807 0.280 15 89326678 frameshift variant A/- delins 0.700 1.000 3 2010 2017
Eczema
CUI: C0013595
Disease: Eczema
368 0.807 0.280 15 89326678 frameshift variant A/- delins 0.700 1.000 3 2010 2017
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.807 0.280 15 89326678 frameshift variant A/- delins 0.700 1.000 3 2010 2017
Isolated somatotropin deficiency
CUI: C3714796
Disease: Isolated somatotropin deficiency
27 0.807 0.280 15 89326678 frameshift variant A/- delins 0.700 1.000 3 2010 2017
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1
CUI: C1834846
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1
13 0.807 0.280 15 89326678 frameshift variant A/- delins 0.700 1.000 3 2010 2017