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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC88C
(P2009L)
Single nucleotide variant
(missense variant)
Hydrocephalus, nonsyndromic, autosomal recessive 1
+3 more
GUncertain significance
CCDC88C
Single nucleotide variant
(intron variant)
not provided
GLikely benign