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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPG7
(A510V)
Single nucleotide variant
(missense variant)
SPG7-related condition
+11 more
GPathogenic/Likely pathogenic
CHCHD10
(R15L)
Single nucleotide variant
(missense variant)
Lower motor neuron syndrome with late-adult onset
+2 more
GPathogenic