rs121912498, RUNX1

N. diseases: 1
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 34886866 missense variant T/C snv 0.700 1.000 3 2002 2013