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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IBA57
(L78V)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 74
GUncertain significance
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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