ClinVar Miner

Submissions for variant NM_017841.4(SDHAF2):c.261-42G>A

gnomAD frequency: 0.70822  dbSNP: rs879647
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000248502 SCV000313037 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001651225 SCV001869475 benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807190 SCV002054686 benign Paragangliomas 2 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001651225 SCV005324411 benign not provided criteria provided, single submitter not provided

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