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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDFY3
Single nucleotide variant
(splice donor variant)
Microcephaly 18, primary, autosomal dominant
GLikely pathogenic
WDFY3
(V2433fs)
Insertion
(frameshift variant)
Microcephaly 18, primary, autosomal dominant
GPathogenic