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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EPS8
(F444L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
GJB2
(G12fs)
Deletion
Nonsyndromic genetic hearing loss
TRIOBP
(R1344Q)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
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