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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPG7, LOC130059818
(A2T)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 7
+3 more
GConflicting classifications of pathogenicity
SPG7, LOC130059818
(L7M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130059818, SPG7
(P27R)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 7
+2 more
GUncertain significance
SPG7, LOC130059818
(E54G)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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