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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSPD1
Deletion
(intron variant)
not provided
GUncertain significance
HSPD1
(A480V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HSPD1
(A365D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HSPD1
(R142K)
Single nucleotide variant
(missense variant)
Spastic paraplegia
+1 more
GConflicting classifications of pathogenicity
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