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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDFY3, WDFY3-AS1
(R783C)
Single nucleotide variant
(missense variant)
Microcephaly 18, primary, autosomal dominant
GUncertain significance
WDFY3, WDFY3-AS1
(T761M)
Single nucleotide variant
(missense variant)
Microcephaly 18, primary, autosomal dominant
GLikely benign