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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RLBP1
(R151Q)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
RLBP1
(S149F)
Single nucleotide variant
(missense variant)
Autosomal recessive retinitis pigmentosa
GPathogenic
RLBP1
Deletion
(inframe_deletion)
Bothnia retinal dystrophy
+3 more
GPathogenic/Likely pathogenic
RLBP1
Deletion
Autosomal recessive retinitis pigmentosa
GPathogenic
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