rs121913616, MPL

N. diseases: 8
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.
Myelofibrosis
CUI: C0026987
Disease: Myelofibrosis
7 0.790 0.120 1 43349337 missense variant TG/AA mnv 0.810 1.000 3 2006 2009
Primary Myelofibrosis
CUI: C0001815
Disease: Primary Myelofibrosis
29 0.790 0.120 1 43349337 missense variant TG/AA mnv 0.050 1.000 5 2009 2014
Thrombocythemia, Essential
CUI: C0040028
Disease: Thrombocythemia, Essential
37 0.790 0.120 1 43349337 missense variant TG/AA mnv 0.040 1.000 4 2009 2015
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 0.790 0.120 1 43349337 missense variant TG/AA mnv 0.020 1.000 2 2008 2009
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.790 0.120 1 43349337 missense variant TG/AA mnv 0.020 1.000 2 2009 2017
Familial thrombocytosis
CUI: C4303761
Disease: Familial thrombocytosis
5 0.790 0.120 1 43349337 missense variant TG/AA mnv 0.010 1.000 1 2009 2009
Polycythemia Vera
CUI: C0032463
Disease: Polycythemia Vera
38 0.790 0.120 1 43349337 missense variant TG/AA mnv 0.010 1.000 1 2009 2009
secondary acute myeloid leukemia
CUI: C0280449
Disease: secondary acute myeloid leukemia
8 0.790 0.120 1 43349337 missense variant TG/AA mnv 0.010 1.000 1 2009 2009