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Variant Pathogenicity
ELAVL2
Name
ELAVL2
HGNC ID
HGNC:3313
Cytogenetic Location
9p21.3
Haploinsufficiency
Minimal Evidence
Triplosensitivity
No Evidence
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ClinVar Variants
ELAVL2
Curated by
Classification
Date
Report
Dosage Sensitivity
Minimal Evidence for Haploinsufficiency
11/28/2018
View report
No Evidence for Triplosensitivity
11/28/2018
View report
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