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.
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.851 0.080 9 5089726 missense variant C/A;T snv 0.700 1.000 1 2010 2010
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 0.851 0.080 9 5089726 missense variant C/A;T snv 0.010 1.000 1 2011 2011
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.851 0.080 9 5089726 missense variant C/A;T snv 0.010 1.000 1 2019 2019
Thrombocythemia, Essential
CUI: C0040028
Disease: Thrombocythemia, Essential
37 0.851 0.080 9 5089726 missense variant C/A;T snv 0.010 1.000 1 2019 2019
Thrombocytosis
CUI: C0836924
Disease: Thrombocytosis
12 0.851 0.080 9 5089726 missense variant C/A;T snv 0.010 1.000 1 2019 2019