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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATL1
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign
ATL1
Single nucleotide variant
(synonymous variant)
Hereditary spastic paraplegia 3A
+2 more
GBenign/Likely benign
ATL1
Single nucleotide variant
(intron variant)
Hereditary spastic paraplegia 3A
+3 more
GBenign/Likely benign
ATL1
Deletion
(splice donor variant)
Hereditary spastic paraplegia 3A
+1 more
GUncertain significance
ATL1
Single nucleotide variant
(synonymous variant)
Hereditary spastic paraplegia
+5 more
GBenign/Likely benign
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