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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KIF5A
(R369W +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+5 more
GConflicting classifications of pathogenicity
KIF5A
Single nucleotide variant
(intron variant)
Spastic paraplegia
+1 more
GUncertain significance