ClinVar Miner

Submissions for variant NM_017841.2(SDHAF2):c.6G>A (p.Ala2=) (rs747571875)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000557765 SCV000637901 likely benign Hereditary Paraganglioma-Pheochromocytoma Syndromes 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000574509 SCV000675046 likely benign Hereditary cancer-predisposing syndrome 2017-06-15 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign

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