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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FA2H
(S322L)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 35
+3 more
GConflicting classifications of pathogenicity
FA2H
(R189*)
Single nucleotide variant
(nonsense)
Inborn genetic diseases
+2 more
GPathogenic