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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RLBP1
(R216Q)
Single nucleotide variant
(missense variant)
Newfoundland cone-rod dystrophy
+4 more
GUncertain significance
RLBP1
(I201T)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+4 more
GConflicting classifications of pathogenicity