ClinVar Miner

Submissions for variant NM_024079.5(ALG8):c.674-29T>C

gnomAD frequency: 0.21953  dbSNP: rs572693
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000249542 SCV000314248 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001711832 SCV001942939 benign not provided 2018-07-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001711832 SCV005235834 benign not provided criteria provided, single submitter not provided

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