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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSPD1
Single nucleotide variant
(synonymous variant)
Hereditary spastic paraplegia
+6 more
GBenign/Likely benign
HSPD1
(D149H)
Single nucleotide variant
(missense variant)
Spastic paraplegia
+2 more
GUncertain significance