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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
USH2A
(V3612I)
Single nucleotide variant
(missense variant)
Usher syndrome type 2
+4 more
GUncertain significance
USH2A
(Y2596C)
Single nucleotide variant
(missense variant)
Usher syndrome type 2
+5 more
GUncertain significance
ADGRV1
(I1669V)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
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