ClinVar Miner

Submissions for variant NM_001851.6(COL9A1):c.1665+13A>T

dbSNP: rs748805630
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000842581 SCV000984605 likely benign not provided 2018-04-30 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV000842581 SCV002395761 benign not provided 2024-06-13 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004702471 SCV005203118 likely benign not specified 2024-07-09 criteria provided, single submitter clinical testing

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