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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSPD1
(G571V)
Single nucleotide variant
(missense variant)
Spastic paraplegia
+1 more
GConflicting classifications of pathogenicity
HSPD1
(M316T)
Single nucleotide variant
(missense variant)
Hypomyelinating leukodystrophy 4
GUncertain significance
HSPD1
(L291V)
Single nucleotide variant
(missense variant)
Spastic paraplegia
+1 more
GConflicting classifications of pathogenicity
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