ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.1274T>G (p.Val425Gly)

dbSNP: rs200047573
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000195027 SCV000248836 uncertain significance not specified 2014-06-10 criteria provided, single submitter clinical testing
Counsyl RCV000663178 SCV000786345 uncertain significance Paragangliomas 5 2018-04-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004692797 SCV005190362 uncertain significance not provided criteria provided, single submitter not provided

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