ClinGen Knowledge Base | Clinical Genome Resource

SDHAF2

Name: SDHAF2
HGNC ID: HGNC:26034
Cytogenetic Location: 11q12.2
Haploinsufficiency: Some Evidence
Triplosensitivity: No Evidence

External Resources: View external resources
ClinVar Variants: View ClinVar Variants
GeneReviews®: View GeneReviews

SDHAF2 - paragangliomas 2 | MONDO:0011121

Curated by	Classification	Date	Report
Clinical Actionability	View report for scoring details	09/07/2018	View report

SDHAF2 - hereditary pheochromocytoma-paraganglioma | MONDO:0017366

Curated by	Classification	Date	Report
Gene-Disease Validity	Definitive	06/22/2017	View report

SDHAF2

Curated by	Classification	Date	Report
Gene Dosage Sensitivity	Some Evidence for Haploinsufficiency	05/31/2017	View report
Gene Dosage Sensitivity	No Evidence for Triplosensitivity	05/31/2017	View report

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