ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.896-20A>G

gnomAD frequency: 0.25110  dbSNP: rs7710005
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000242256 SCV000310007 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001711814 SCV001159392 benign not provided 2020-01-03 criteria provided, single submitter clinical testing
GeneDx RCV001711814 SCV001944491 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316407 SCV004015379 benign Paragangliomas 5 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001711814 SCV005302884 benign not provided criteria provided, single submitter not provided

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