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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRSS56
(Q356fs +1 more)
Duplication
(frameshift variant)
PRSS56-related disorder
+3 more
GPathogenic/Likely pathogenic
PRSS56
(R467L +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity