ClinVar Miner

Submissions for variant NM_000093.5(COL5A1):c.2031G>T (p.Glu677Asp)

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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 RCV002592946 SCV002942172 benign Ehlers-Danlos syndrome, classic type, 1 2022-06-27 criteria provided, single submitter clinical testing

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