ClinVar Miner

Submissions for variant NM_017841.4(SDHAF2):c.260+10T>G

dbSNP: rs1590764949
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001477781 SCV001682029 likely benign Hereditary pheochromocytoma-paraganglioma 2018-07-12 criteria provided, single submitter clinical testing

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