ClinVar Miner

Submissions for variant NM_017841.2(SDHAF2):c.21C>T (p.Phe7=) (rs892955355)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000461014 SCV000562731 likely benign Hereditary Paraganglioma-Pheochromocytoma Syndromes 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV001014772 SCV001175526 likely benign Hereditary cancer-predisposing syndrome 2018-05-09 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign

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