Source: INFERRED ×
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.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
0.851 0.280 11 108331498 missense variant G/C;T snv 2.4E-05 7.0E-06 0.700 1.000 7 2000 2012
Ataxia Telangiectasia
CUI: C0004135
Disease: Ataxia Telangiectasia
0.851 0.280 11 108331498 missense variant G/C;T snv 2.4E-05 7.0E-06 0.700 0