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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FECH
Single nucleotide variant
(intron variant)
not provided
+2 more
GConflicting classifications of pathogenicity
FECH
(R102* +2 more)
Single nucleotide variant
(nonsense)
Protoporphyria, erythropoietic, 1
+1 more
GPathogenic/Likely pathogenic