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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OPHN1
(L638P)
Single nucleotide variant
(missense variant)
X-linked intellectual disability-cerebellar hypoplasia syndrome
GUncertain significance
OPHN1
(E361fs)
Insertion
(frameshift variant)
X-linked intellectual disability-cerebellar hypoplasia syndrome
GLikely pathogenic
OPHN1
(K254R)
Single nucleotide variant
(missense variant)
X-linked intellectual disability-cerebellar hypoplasia syndrome
GUncertain significance
OPHN1
(R147G)
Single nucleotide variant
(missense variant)
X-linked intellectual disability-cerebellar hypoplasia syndrome
GPathogenic
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