RS1060499616 RUNX1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1
Inherited bleeding disorder
platelet-type
Hereditary thrombocytopenia and hematologic cancer predisposition syndrome
RUNX1-related disorder
Inborn genetic diseases
Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1
Inherited bleeding disorder
platelet-type
Hereditary thrombocytopenia and hematologic cancer predisposition syndrome
RUNX1-related disorder
Inborn genetic diseases
Other Variants in RUNX1