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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC108021846, SOX9
(S23fs)
Deletion
(frameshift variant)
Connective tissue disorder
GLikely pathogenic
LOC108021846, SOX9
(R107Q)
Single nucleotide variant
(missense variant)
Connective tissue disorder
GUncertain significance