ClinVar Miner

Submissions for variant NM_000088.4(COL1A1):c.2507G>A (p.Gly836Asp)

dbSNP: rs72653130
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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 RCV002277890 SCV002565158 likely pathogenic Osteogenesis imperfecta 2018-10-24 criteria provided, single submitter clinical testing

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