rs74315450, RUNX1

N. diseases: 5
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.
Platelet Disorder, Familial, with Associated Myeloid Malignancy
CUI: C1832388
Disease: Platelet Disorder, Familial, with Associated Myeloid Malignancy
20 0.851 0.120 21 34859485 missense variant C/T snv 0.800 1.000 9 1999 2017
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.851 0.120 21 34859485 missense variant C/T snv 0.020 1.000 2 2012 2015
leukemia
CUI: C0023418
Disease: leukemia
144 0.851 0.120 21 34859485 missense variant C/T snv 0.020 1.000 2 2012 2015
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.851 0.120 21 34859485 missense variant C/T snv 0.010 1.000 1 2010 2010
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
110 0.851 0.120 21 34859485 missense variant C/T snv 0.010 1.000 1 2015 2015