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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SNRNP200
(A787T)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 33
+2 more
GPathogenic/Likely pathogenic
SNRNP200
(R681C)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+3 more
GPathogenic/Likely pathogenic