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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALDH18A1
(D623N +5 more)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 9A
+6 more
GUncertain significance
ALDH18A1
(S469R +5 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GUncertain significance
ALDH18A1
Single nucleotide variant
(synonymous variant)
Hereditary spastic paraplegia
+7 more
GBenign/Likely benign
ALDH18A1
(S372Y +5 more)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia
+7 more
GBenign
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