ClinVar Miner

Submissions for variant NM_001853.4(COL9A3):c.685-4G>T

dbSNP: rs57739618
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252757 SCV000308432 benign not specified criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000252757 SCV000336936 benign not specified 2015-11-09 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000252757 SCV001475627 benign not specified 2020-07-09 criteria provided, single submitter clinical testing
Invitae RCV001517330 SCV001725810 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001517330 SCV001845309 benign not provided 2018-07-15 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001517330 SCV001798182 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV000252757 SCV001807056 benign not specified no assertion criteria provided clinical testing

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