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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PEX6
(F714fs +1 more)
Deletion
(frameshift variant +1 more)
Heimler syndrome 2
GLikely pathogenic
PEX6
(G220V)
Single nucleotide variant
(missense variant +2 more)
Heimler syndrome 2
+4 more
GConflicting classifications of pathogenicity