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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FECH
(E207K +3 more)
Single nucleotide variant
(missense variant)
Protoporphyria, erythropoietic, 1
+1 more
GConflicting classifications of pathogenicity
FECH
(R115* +2 more)
Single nucleotide variant
(nonsense)
Protoporphyria, erythropoietic, 1
+1 more
GPathogenic/Likely pathogenic
FECH
(T69fs +1 more)
Duplication
(frameshift variant +1 more)
Protoporphyria, erythropoietic, 1
GPathogenic
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