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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FUS
Single nucleotide variant
(synonymous variant +1 more)
not specified
+3 more
GBenign
FUS
Single nucleotide variant
(synonymous variant +1 more)
Tremor, hereditary essential, 4
+3 more
GBenign
FUS
Duplication
(intron variant)
not provided
GLikely benign
FUS
Deletion
(intron variant)
not specified
+1 more
GBenign/Likely benign
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