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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PEX5
(N489K +7 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
PEX5
(L562fs +6 more)
Duplication
(frameshift variant)
Rhizomelic chondrodysplasia punctata type 5
GLikely pathogenic