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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STX16, STX16-NPEPL1
(V119M +4 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
STX16-related disorder
GUncertain significance
STX16, STX16-NPEPL1
Single nucleotide variant
(non-coding transcript variant +1 more)
STX16-related disorder
GLikely benign