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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C19orf12
(P72L +1 more)
Single nucleotide variant
(missense variant)
Neurodegeneration with brain iron accumulation 4
GLikely pathogenic
C19orf12
(L51P)
Single nucleotide variant
(missense variant +2 more)
Hereditary spastic paraplegia 43
GLikely pathogenic