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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETX
(V919L)
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 4
+4 more
GConflicting classifications of pathogenicity
SETX
(L804S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity