ClinVar Miner

Submissions for variant NM_002382.5(MAX):c.426G>A (p.Ser142=) (rs145787299)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000474580 SCV000554473 likely benign Hereditary Paraganglioma-Pheochromocytoma Syndromes 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000568431 SCV000673598 likely benign Hereditary cancer-predisposing syndrome 2015-11-03 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign

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