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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130059818, SPG7
(M1V)
Single nucleotide variant
(missense variant +1 more)
SPG7-related condition
+2 more
GPathogenic/Likely pathogenic
LOC130059818, SPG7
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GConflicting classifications of pathogenicity