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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IMPG2
(C1038F)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+1 more
GConflicting classifications of pathogenicity
IMPG2
(E745fs)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic
IMPG2
(W137*)
Single nucleotide variant
(nonsense)
Retinitis pigmentosa 56
+2 more
GPathogenic/Likely pathogenic
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