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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDR62
(R512L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
WDR62
(E531fs)
Duplication
(frameshift variant)
Microcephaly 2, primary, autosomal recessive, with or without cortical malformations
GLikely pathogenic