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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130064702, RTN2
Microsatellite
(5 prime UTR variant)
Hereditary spastic paraplegia
+1 more
GConflicting classifications of pathogenicity
LOC130064702, RTN2
Microsatellite
(5 prime UTR variant)
not provided
+1 more
GConflicting classifications of pathogenicity