ClinVar Miner

Submissions for variant NM_001851.6(COL9A1):c.1143+14T>G

dbSNP: rs1562317487
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002091613 SCV002440079 likely benign not provided 2021-12-08 criteria provided, single submitter clinical testing

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