RS1057519750 RUNX1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Acute myeloid leukemia
Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1
Hereditary thrombocytopenia and hematologic cancer predisposition syndrome
Inborn genetic diseases
Acute myeloid leukemia
Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1
Hereditary thrombocytopenia and hematologic cancer predisposition syndrome
Inborn genetic diseases
Other Variants in RUNX1