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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS37A
(Q47L +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary spastic paraplegia 53
GUncertain significance
VPS37A
(L234I +2 more)
Single nucleotide variant
(missense variant)
Idiopathic transverse myelitis
+1 more
GConflicting classifications of pathogenicity