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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NLGN4X
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GBenign/Likely benign
NLGN4X
(P63T)
Single nucleotide variant
(missense variant)
Asperger syndrome, X-linked, susceptibility to, 2
+2 more
GUncertain significance