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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PEX7
(R232*)
Single nucleotide variant
(nonsense)
Rhizomelic chondrodysplasia punctata type 1
+2 more
GPathogenic
PEX7
Single nucleotide variant
(splice donor variant)
PEX7-related disorder
+4 more
GPathogenic