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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ESPN
(D304Y)
Single nucleotide variant
(missense variant)
Sensorineural hearing loss disorder
GUncertain significance
CDC14A
(A158fs +2 more)
Deletion
(frameshift variant)
Sensorineural hearing loss disorder
GPathogenic