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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OPHN1
(I527V)
Single nucleotide variant
(missense variant)
X-linked intellectual disability-cerebellar hypoplasia syndrome
GUncertain significance
OPHN1
Single nucleotide variant
(splice donor variant)
X-linked intellectual disability-cerebellar hypoplasia syndrome
GLikely pathogenic
OPHN1
(L64P)
Single nucleotide variant
(missense variant)
X-linked intellectual disability-cerebellar hypoplasia syndrome
GUncertain significance
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