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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CENPJ, RNF17
(E1235V)
Single nucleotide variant
(missense variant +1 more)
Microcephaly 6, primary, autosomal recessive
GPathogenic
CENPJ, RNF17
Single nucleotide variant
(splice acceptor variant)
Microcephaly 6, primary, autosomal recessive
GPathogenic