ClinVar Miner

Submissions for variant NM_052845.4(MMAB):c.584+24A>G

gnomAD frequency: 0.07842  dbSNP: rs78599682
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244449 SCV000315239 likely benign not specified criteria provided, single submitter clinical testing
Pars Genome Lab RCV001533429 SCV001750019 likely benign Methylmalonic aciduria, cblB type 2021-07-01 criteria provided, single submitter clinical testing
GeneDx RCV001610743 SCV001833421 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001610743 SCV005218758 likely benign not provided criteria provided, single submitter not provided

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