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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLPP2
(P228S +2 more)
Single nucleotide variant
(missense variant)
PLPP2-related disorder
GLikely benign
PLPP2
(C185R +2 more)
Single nucleotide variant
(missense variant)
PLPP2-related disorder
GLikely benign