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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IMPG2
(L939H)
Single nucleotide variant
(missense variant)
Vitelliform macular dystrophy 5
GLikely pathogenic
IMPG2
(V609fs)
Deletion
(frameshift variant)
Retinitis pigmentosa 56
GPathogenic
IMPG2
Single nucleotide variant
(splice donor variant)
Retinitis pigmentosa 56
GPathogenic
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