ClinVar Miner

Submissions for variant NM_003001.5(SDHC):c.21-211C>T

gnomAD frequency: 0.11557  dbSNP: rs4255402
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001691453 SCV001913216 benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001691453 SCV005285770 benign not provided criteria provided, single submitter not provided

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