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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEP164
(P157fs)
Deletion
(frameshift variant)
Retinal dystrophy
GLikely pathogenic
CEP164
(Q1410* +1 more)
Single nucleotide variant
(nonsense)
not specified
+3 more
GConflicting classifications of pathogenicity