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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRIOBP
(D52N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TRIOBP
(G2183D +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive nonsyndromic hearing loss 28
GUncertain significance