ClinVar Miner

Submissions for variant NM_000493.4(COL10A1):c.720G>A (p.Pro240=)

dbSNP: rs112875740
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000299394 SCV000333281 uncertain significance not provided 2015-08-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000299394 SCV002398706 likely benign not provided 2022-09-02 criteria provided, single submitter clinical testing

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