rs1569061768, RUNX1

N. diseases: 2
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 1.000 0.120 21 34859477 stop gained G/A snv 0.700 1.000 1 1999 1999
Thrombocytopenia
CUI: C0040034
Disease: Thrombocytopenia
110 1.000 0.120 21 34859477 stop gained G/A snv 0.700 0