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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC35A3
(R67H +1 more)
Single nucleotide variant
(missense variant)
Autism spectrum disorder - epilepsy - arthrogryposis syndrome
GUncertain significance
SLC35A3
(S296G +1 more)
Single nucleotide variant
(missense variant +1 more)
Autism spectrum disorder - epilepsy - arthrogryposis syndrome
+1 more
GPathogenic