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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLPP
Single nucleotide variant
(5 prime UTR variant)
not specified
+2 more
GBenign
CLPP, LOC130063288
Duplication
(intron variant)
Perrault syndrome 3
+1 more
GBenign