rs201478192, KIDINS220

N. diseases: 12
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.
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
47 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.070 1.000 7 2006 2019
Myeloproliferative disease
CUI: C0027022
Disease: Myeloproliferative disease
43 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.070 0.857 7 2006 2019
Thrombocythemia, Essential
CUI: C0040028
Disease: Thrombocythemia, Essential
37 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.050 1.000 5 2009 2015
Polycythemia Vera
CUI: C0032463
Disease: Polycythemia Vera
38 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.040 1.000 4 2013 2015
Primary Myelofibrosis
CUI: C0001815
Disease: Primary Myelofibrosis
29 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.040 1.000 4 2007 2015
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.020 1.000 2 2007 2013
Lymphoproliferative Disorders
CUI: C0024314
Disease: Lymphoproliferative Disorders
14 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.010 1 2007 2007
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.010 1.000 1 2007 2007
Monoclonal Gammopathy of Undetermined Significance
CUI: C0026470
Disease: Monoclonal Gammopathy of Undetermined Significance
20 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.010 1.000 1 2007 2007
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.010 1.000 1 2007 2007
Myelofibrosis
CUI: C0026987
Disease: Myelofibrosis
7 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.010 1.000 1 2007 2007
Neoplasm, Residual
CUI: C0242596
Disease: Neoplasm, Residual
23 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 0.010 1.000 1 2009 2009