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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHST3
Inversion
(splice acceptor variant)
Spondyloepiphyseal dysplasia with congenital joint dislocations
GLikely pathogenic
CHST3
(R370H)
Single nucleotide variant
(missense variant)
Spondyloepiphyseal dysplasia with congenital joint dislocations
GUncertain significance