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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130057872, RLBP1
Deletion
Retinal dystrophy
+1 more
GLikely pathogenic
RLBP1
(M226K)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa
+3 more
GPathogenic