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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAB28
(C217W)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
RAB28
(Q189*)
Single nucleotide variant
(nonsense)
Cone-rod dystrophy 18
GPathogenic
RAB28
(R137*)
Single nucleotide variant
(nonsense)
Cone-rod dystrophy 18
+1 more
GPathogenic
RAB28
Single nucleotide variant
(splice donor variant)
Cone-rod dystrophy 18
GPathogenic
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