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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C10orf105, CDH23
(T1209A)
Single nucleotide variant
(missense variant +1 more)
Usher syndrome
GBenign
C10orf105, CDH23
(R1334W)
Single nucleotide variant
(missense variant +1 more)
Usher syndrome
GUncertain significance