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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SAG
(R193*)
Single nucleotide variant
(nonsense)
Retinal dystrophy
+4 more
GPathogenic
SAG
(V245M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance