ClinVar Miner

Submissions for variant NM_000094.4(COL7A1):c.5117G>A (p.Gly1706Glu)

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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 RCV004690848 SCV005186122 uncertain significance not specified 2024-05-01 criteria provided, single submitter clinical testing

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