ClinVar Miner

Submissions for variant NM_000094.4(COL7A1):c.4786C>T (p.Pro1596Ser)

dbSNP: rs2531106233
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003490821 SCV004240894 uncertain significance not specified 2023-12-12 criteria provided, single submitter clinical testing

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