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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNGB1
(T836fs +1 more)
Duplication
(frameshift variant)
Retinitis pigmentosa
GLikely pathogenic
CNGB1
Single nucleotide variant
(intron variant)
Retinitis pigmentosa 45
+1 more
GPathogenic/Likely pathogenic