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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC26A4
(V577A)
Single nucleotide variant
(missense variant)
not specified
+4 more
GUncertain significance
SLC26A4
(L597S)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity