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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC88C
(A1793G)
Single nucleotide variant
(missense variant)
Hydrocephalus, nonsyndromic, autosomal recessive 1
+1 more
GConflicting classifications of pathogenicity
CCDC88C
(R574W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity