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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130068340, UBQLN2
Single nucleotide variant
(synonymous variant)
Amyotrophic lateral sclerosis type 15
GBenign
LOC130068340, UBQLN2
(A242T)
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 15
GConflicting classifications of pathogenicity