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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RD3
Single nucleotide variant
(synonymous variant)
Leber congenital amaurosis 12
GBenign
RD3
(W6R)
Single nucleotide variant
(missense variant)
Leber congenital amaurosis 12
GBenign