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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 15 52061301 missense variant C/G snv 5.8E-02 5.9E-02 0.010 1.000 1 2017 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 15 52061301 missense variant C/G snv 5.8E-02 5.9E-02 0.010 1.000 1 2017 2017
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 15 52061301 missense variant C/G snv 5.8E-02 5.9E-02 0.010 1.000 1 2017 2017