RS1325257479 ALDH18A1
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Associated Conditions
Inborn genetic diseases
Autosomal dominant spastic paraplegia type 9
Cutis laxa
autosomal dominant 3
de Barsy syndrome
Autosomal recessive complex spastic paraplegia type 9B
Inborn genetic diseases
Autosomal dominant spastic paraplegia type 9
Cutis laxa
autosomal dominant 3
de Barsy syndrome
Autosomal recessive complex spastic paraplegia type 9B
Other Variants in ALDH18A1