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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHST3
Single nucleotide variant
(synonymous variant)
Larsen-like syndrome, B3GAT3 type
+2 more
GBenign/Likely benign
CHST3
Single nucleotide variant
(synonymous variant)
Spondyloepiphyseal dysplasia with congenital joint dislocations
+3 more
GBenign/Likely benign