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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASPM
(R3308L +1 more)
Single nucleotide variant
(missense variant)
Microcephaly 5, primary, autosomal recessive
GLikely pathogenic
ASPM
(Q1823*)
Single nucleotide variant
(nonsense +1 more)
Microcephaly 5, primary, autosomal recessive
GPathogenic