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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SRPX2
(W58C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SRPX2
(S102L)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
SRPX2
(N327K)
Single nucleotide variant
(missense variant)
Rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
+1 more
GUncertain significance
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