ClinVar Miner

Submissions for variant NM_017841.4(SDHAF2):c.370+12G>A

dbSNP: rs886048415
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000336073 SCV000372664 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002056210 SCV002321579 likely benign Hereditary pheochromocytoma-paraganglioma 2023-11-27 criteria provided, single submitter clinical testing

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