ClinVar Miner

Submissions for variant NM_003002.4(SDHD):c.*260T>A

gnomAD frequency: 0.04112  dbSNP: rs149570245
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000151830 SCV000200301 benign not specified 2013-11-05 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000316201 SCV000367351 benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001668305 SCV001888745 benign not provided 2018-06-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001668305 SCV005231600 benign not provided criteria provided, single submitter not provided

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