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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP5ME, PDE6B
(R799* +2 more)
Single nucleotide variant
(nonsense)
Retinal dystrophy
+3 more
GPathogenic
ATP5ME, PDE6B
Single nucleotide variant
(splice donor variant +1 more)
Retinitis pigmentosa 40
GLikely pathogenic