ClinVar Miner

Submissions for variant NM_017841.2(SDHAF2):c.15A>G (p.Thr5=) (rs144511254)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000475629 SCV000562733 likely benign Hereditary Paraganglioma-Pheochromocytoma Syndromes 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000563732 SCV000675041 likely benign Hereditary cancer-predisposing syndrome 2015-03-09 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV001090317 SCV001245793 likely benign not provided 2019-10-01 criteria provided, single submitter clinical testing

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