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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ELOVL4
Single nucleotide variant
(splice acceptor variant)
not provided
+1 more
GPathogenic/Likely pathogenic
ELOVL4
(P72fs)
Deletion
(frameshift variant)
Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome
+1 more
GConflicting classifications of pathogenicity
ELOVL4
(L55V)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 34
+1 more
GUncertain significance
ERVH-3, ETV7
+427 more
Copy number gain
not provided
GPathogenic
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