ClinVar Miner

Submissions for variant NM_003001.5(SDHC):c.77+32A>T

gnomAD frequency: 0.12478  dbSNP: rs77828459
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001000115 SCV001156545 benign not specified 2019-05-15 criteria provided, single submitter clinical testing
GeneDx RCV001644888 SCV001859423 benign not provided 2019-08-07 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV001000115 SCV002568048 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001644888 SCV005285773 benign not provided criteria provided, single submitter not provided

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