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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130068202, RP2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
RP2
(T87I)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
RP2
(R118fs)
Deletion
(frameshift variant)
not provided
GPathogenic
RP2
(Y198fs)
Deletion
(frameshift variant)
not provided
GPathogenic
RP2
(R211fs)
Deletion
(frameshift variant)
not provided
GPathogenic
RP2
(R282W)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
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