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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TOP3A
(N678D +1 more)
Single nucleotide variant
(missense variant)
Microcephaly, growth restriction, and increased sister chromatid exchange 2
+3 more
GBenign/Likely benign
TOP3A
Single nucleotide variant
(intron variant)
Microcephaly, growth restriction, and increased sister chromatid exchange 2
+2 more
GBenign
TOP3A
Single nucleotide variant
(intron variant)
Microcephaly, growth restriction, and increased sister chromatid exchange 2
+3 more
GBenign/Likely benign
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