RS762890562 DDX41
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What This Variant Does
"CLNSIG=255
Associated Conditions
Acute myeloid leukemia
DDX41-related hematologic malignancy predisposition syndrome
DDX41-related disorder
Inborn genetic diseases
Acute myeloid leukemia
DDX41-related hematologic malignancy predisposition syndrome
DDX41-related disorder
Inborn genetic diseases
Other Variants in DDX41