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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NONO
(R64* +1 more)
Single nucleotide variant
(nonsense)
Syndromic X-linked intellectual disability 34
GPathogenic
NONO
(R184* +1 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
NONO
Single nucleotide variant
(splice donor variant)
Syndromic X-linked intellectual disability 34
GPathogenic
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