ClinVar Miner

Submissions for variant NM_001853.4(COL9A3):c.901-9T>C

gnomAD frequency: 0.00695  dbSNP: rs74506912
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000175296 SCV000226762 benign not specified 2014-10-20 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000175296 SCV000308439 benign not specified criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000991659 SCV001143306 benign not provided 2019-02-20 criteria provided, single submitter clinical testing
Invitae RCV000991659 SCV001730818 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV000991659 SCV001841123 benign not provided 2018-09-18 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002277352 SCV002566454 benign Connective tissue disorder 2022-05-26 criteria provided, single submitter clinical testing

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