rs1057519748, RUNX1

N. diseases: 2
Source: CLINVAR ×
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
19 0.827 0.120 21 34859486 stop gained G/A snv 0.700 1.000 4 1999 2017
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
141 0.827 0.120 21 34859486 stop gained G/A snv 0.700 1.000 1 1999 1999