ClinVar Miner

Submissions for variant NM_001379500.1(COL18A1):c.2684-14TC[2]

dbSNP: rs148455528
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514818 SCV000610326 likely benign not provided 2017-03-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000514818 SCV001728241 benign not provided 2025-02-02 criteria provided, single submitter clinical testing

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