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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC26A2
(R492W)
Single nucleotide variant
(missense variant)
Connective tissue disorder
+7 more
GBenign/Likely benign
SLC26A2
(I574T)
Single nucleotide variant
(missense variant)
Connective tissue disorder
+7 more
GBenign
SLC26A2
(T689S)
Single nucleotide variant
(missense variant)
Connective tissue disorder
+7 more
GBenign/Likely benign
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