ClinVar Miner

Submissions for variant NM_001853.4(COL9A3):c.275G>C (p.Gly92Ala)

dbSNP: rs1991064282
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002278705 SCV002566437 uncertain significance Connective tissue disorder 2021-11-25 criteria provided, single submitter clinical testing

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