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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPG11, EIF3J
Duplication
(3 prime UTR variant)
Spastic Paraplegia, Recessive
GUncertain significance
EIF3J, SPG11
Single nucleotide variant
(3 prime UTR variant)
Hereditary spastic paraplegia 11
GUncertain significance
EIF3J, SPG11
Duplication
(3 prime UTR variant)
Spastic Paraplegia, Recessive
GUncertain significance
EIF3J, SPG11
Single nucleotide variant
(3 prime UTR variant)
Spastic Paraplegia, Recessive
GUncertain significance
ADAL, AFG2B
+103 more
Deletion
not provided
GPathogenic
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