RS779626155 DNMT3A
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What This Variant Does
"CLNSIG=5
Associated Conditions
Tatton-Brown-Rahman overgrowth syndrome
Acute myeloid leukemia
Inborn genetic diseases
Tatton-Brown-Rahman overgrowth syndrome
Tatton-Brown-Rahman overgrowth syndrome
Acute myeloid leukemia
Inborn genetic diseases
Tatton-Brown-Rahman overgrowth syndrome
Other Variants in DNMT3A