ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.54T>C (p.Leu18=) (rs759446168)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000872648 SCV001014497 likely benign not provided 2018-10-22 criteria provided, single submitter clinical testing
Ambry Genetics RCV001024191 SCV001186163 likely benign Hereditary cancer-predisposing syndrome 2018-09-04 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Invitae RCV001483271 SCV001687659 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2018-10-22 criteria provided, single submitter clinical testing

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