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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RP2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely pathogenic
RP2
(L53fs)
Deletion
(frameshift variant)
Retinitis pigmentosa 3
GPathogenic
RP2
(T87I)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
RP2
Single nucleotide variant
(intron variant)
Retinitis pigmentosa 3
+3 more
GConflicting classifications of pathogenicity
RP2
(C311fs)
Deletion
(frameshift variant)
Retinitis pigmentosa 3
GPathogenic
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