RS144689354 DNMT3A
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What This Variant Does
"CLNSIG=4
Associated Conditions
Tatton-Brown-Rahman overgrowth syndrome
Acute myeloid leukemia
Heyn-Sproul-Jackson syndrome
Autism spectrum disorder
Neoplasm
Inborn genetic diseases
DNMT3A-related disorder
Pilocytic astrocytoma
Tatton-Brown-Rahman overgrowth syndrome
Acute myeloid leukemia
Heyn-Sproul-Jackson syndrome
Autism spectrum disorder
Neoplasm
Inborn genetic diseases
DNMT3A-related disorder
Other Variants in DNMT3A