RS766264810 ALDH18A1

Health Risk Chr 10:95611372
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary spastic paraplegia 9A
Cutis laxa
autosomal dominant 3
de Barsy syndrome
Autosomal dominant spastic paraplegia type 9
Hereditary spastic paraplegia 9A
Cutis laxa
autosomal dominant 3
de Barsy syndrome
Autosomal dominant spastic paraplegia type 9
Other Variants in ALDH18A1
rs121434582 rs121434583 rs863223315 rs587777858 rs786205614 rs537043237 rs752669339 rs864321669 rs864321670 rs863224945
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