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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
USH2A
(E767fs)
Deletion
(frameshift variant)
Retinitis pigmentosa 39
+23 more
GConflicting classifications of pathogenicity
SHH
(G29A)
Single nucleotide variant
(missense variant)
Anemia
+9 more
GUncertain significance