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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PDZD7
(Q737fs)
Deletion
(frameshift variant)
Nonsyndromic genetic hearing loss
+1 more
GPathogenic/Likely pathogenic
PDZD7
(R56fs)
Duplication
(frameshift variant)
not provided
+2 more
GPathogenic