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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FECH
Single nucleotide variant
(intron variant)
Autosomal erythropoietic protoporphyria
+2 more
GConflicting classifications of pathogenicity
FECH, LOC130062555
Single nucleotide variant
(intron variant)
Protoporphyria, erythropoietic, 1
+1 more
GConflicting classifications of pathogenicity