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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZDHHC9
(L189P)
Single nucleotide variant
(missense variant)
Syndromic X-linked intellectual disability Raymond type
GUncertain significance
ZDHHC9
(R182C)
Single nucleotide variant
(missense variant)
Syndromic X-linked intellectual disability Raymond type
GConflicting classifications of pathogenicity