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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEP55
(H378L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign
CEP55
Single nucleotide variant
(intron variant)
Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome
+1 more
GBenign