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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP4V2
(G95R)
Single nucleotide variant
(missense variant)
Bietti crystalline corneoretinal dystrophy
+2 more
GPathogenic/Likely pathogenic
CYP4V2
(M123V)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
CYP4V2
(R232*)
Single nucleotide variant
(nonsense)
Retinal dystrophy
+2 more
GPathogenic
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