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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IBA57
(P89L)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 74
+2 more
GUncertain significance
IBA57
(A91G)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 74
+1 more
GUncertain significance
IBA57
(R83H +1 more)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 74
+2 more
GUncertain significance
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