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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC26A2
(A147fs)
Duplication
(frameshift variant)
Atelosteogenesis type II
+3 more
GPathogenic/Likely pathogenic
SLC26A2
(I607fs)
Deletion
(frameshift variant)
Diastrophic dysplasia
GUncertain significance