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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GJB2
(G12fs)
Deletion
Nonsyndromic genetic hearing loss
GPathogenic
MYO1F
(R594Q +1 more)
Single nucleotide variant
(missense variant)
Bilateral sensorineural hearing impairment
GUncertain significance