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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCGN
Deletion
(splice acceptor variant)
SCGN-related disorder
+1 more
GBenign
SCGN
(L150Q)
Single nucleotide variant
(missense variant)
SCGN-related disorder
GLikely benign