ClinVar Miner

Submissions for variant NM_001854.4(COL11A1):c.2976T>C (p.Pro992=)

dbSNP: rs368868551
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000594065 SCV000703483 uncertain significance not provided 2016-12-19 criteria provided, single submitter clinical testing
GeneDx RCV000594065 SCV001819215 likely benign not provided 2020-06-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000594065 SCV002403931 likely benign not provided 2024-06-03 criteria provided, single submitter clinical testing

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