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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BRWD3
(K1288R)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 93
+2 more
GBenign
BRWD3
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
BRWD3
Duplication
(intron variant)
not provided
+1 more
GBenign
BRWD3
Duplication
(intron variant)
not provided
+1 more
GBenign
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