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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AP1S3
(T32I)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
AP1S3, LOC129935691
Single nucleotide variant
(intron variant)
AP1S3-related disorder
GLikely benign