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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
USH2A
(W3955*)
Single nucleotide variant
(nonsense)
Usher syndrome type 3A
+10 more
GPathogenic
USH2A
(G3142*)
Single nucleotide variant
(nonsense)
Usher syndrome type 2A
+7 more
GPathogenic/Likely pathogenic