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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DIS3L2
(G18fs)
Deletion
(frameshift variant +2 more)
Perlman syndrome
GLikely pathogenic
DIS3L2
(R576H)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GConflicting classifications of pathogenicity