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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SOX3
Deletion
(inframe_deletion)
not specified
+4 more
GBenign/Likely benign
LOC108281134, SOX3
(R5Q)
Single nucleotide variant
(missense variant)
not specified
+4 more
GBenign/Likely benign