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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC35A3
(D14G)
Single nucleotide variant
(missense variant +1 more)
Autism spectrum disorder - epilepsy - arthrogryposis syndrome
+1 more
GBenign
SLC35A3
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign