RS377577594 DNMT3A
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What This Variant Does
"CLNSIG=5
Associated Conditions
Acute myeloid leukemia
Tatton-Brown-Rahman overgrowth syndrome
Inborn genetic diseases
Neurodevelopmental disorder
EBV-positive nodal T- and NK-cell lymphoma
DNMT3A-related disorder
Neoplasm
Heyn-Sproul-Jackson syndrome
Tatton-Brown-Rahman overgrowth syndrome
Acute myeloid leukemia
Tatton-Brown-Rahman overgrowth syndrome
Inborn genetic diseases
Neurodevelopmental disorder
EBV-positive nodal T- and NK-cell lymphoma
DNMT3A-related disorder
Other Variants in DNMT3A