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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
USH2A, USH2A-AS1
(S1369L)
Single nucleotide variant
(missense variant)
Usher syndrome
+6 more
GConflicting classifications of pathogenicity
USH2A, USH2A-AS1
(N1343H)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+4 more
GUncertain significance
USH2A, USH2A-AS1
Single nucleotide variant
(splice acceptor variant)
Retinitis pigmentosa
GLikely pathogenic
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