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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNMT3A
(R749C +3 more)
Single nucleotide variant
(missense variant +1 more)
Tatton-Brown-Rahman overgrowth syndrome
GPathogenic
DNMT3A
(F191fs +3 more)
Duplication
(frameshift variant +1 more)
Inborn genetic diseases
GPathogenic