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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHST3
(H214Q)
Single nucleotide variant
(missense variant)
Spondyloepiphyseal dysplasia with congenital joint dislocations
GUncertain significance
CHST3
(R221C)
Single nucleotide variant
(missense variant)
Spondyloepiphyseal dysplasia with congenital joint dislocations
+1 more
GLikely pathogenic
CHST3
(G316fs)
Deletion
(frameshift variant)
Spondyloepiphyseal dysplasia with congenital joint dislocations
GUncertain significance
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