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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALDH18A1
(R514H +5 more)
Single nucleotide variant
(missense variant)
Autosomal recessive complex spastic paraplegia type 9B
+5 more
GConflicting classifications of pathogenicity
COL2A1
(A112S +1 more)
Single nucleotide variant
(missense variant)
Spondyloepiphyseal dysplasia, Stanescu type
GBenign