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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ERLIN1
Single nucleotide variant
(synonymous variant +2 more)
Hereditary spastic paraplegia 62
+1 more
GBenign
ERLIN1
Single nucleotide variant
(synonymous variant +2 more)
ERLIN1-related disorder
GLikely benign