ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.73-111G>A

gnomAD frequency: 0.41897  dbSNP: rs9435745
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 RCV001693235 SCV001907368 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001693235 SCV005285516 benign not provided criteria provided, single submitter not provided

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