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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SOD1
(D77V)
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 1
GPathogenic/Likely pathogenic
SOD1
(R116H)
Single nucleotide variant
(missense variant)
Spastic tetraplegia and axial hypotonia, progressive
+2 more
GConflicting classifications of pathogenicity
ATP5PO, C21orf62
+25 more
Copy number loss
not provided
GPathogenic
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