ClinVar Miner

Submissions for variant NM_001379500.1(COL18A1):c.2620+29C>T

gnomAD frequency: 0.16080  dbSNP: rs73370840
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000245327 SCV000314648 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001722342 SCV001947637 benign not provided 2021-05-11 criteria provided, single submitter clinical testing

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