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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IMPG2
(R1088*)
Single nucleotide variant
(nonsense)
Vitelliform macular dystrophy 5
+2 more
GPathogenic/Likely pathogenic
IMPG2
(F1016S)
Single nucleotide variant
(missense variant)
Vitelliform macular dystrophy 5
GLikely pathogenic