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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RLBP1
(F95fs)
Deletion
(frameshift variant)
Pigmentary retinal dystrophy
+2 more
GPathogenic
RLBP1
(R9C)
Single nucleotide variant
(missense variant)
Newfoundland cone-rod dystrophy
+2 more
GConflicting classifications of pathogenicity