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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EXT1
(L490fs)
Deletion
(frameshift variant)
Chondrosarcoma
+3 more
GPathogenic
EXT1
(E326fs)
Deletion
(frameshift variant)
Exostoses, multiple, type 1
GLikely pathogenic
EXT1
(K218N)
Single nucleotide variant
(missense variant)
Exostoses, multiple, type 1
GUncertain significance
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