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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC30A2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
ARID1A, AUNIP
+33 more
Duplication
Retinitis pigmentosa 59
GUncertain significance
AUNIP, CATSPER4
+22 more
Deletion
Hypercholesterolemia, familial, 4
GPathogenic
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