ClinVar Miner

Submissions for variant NM_000093.5(COL5A1):c.4814C>G (p.Ala1605Gly)

dbSNP: rs145175057
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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 RCV002240512 SCV001229713 benign Ehlers-Danlos syndrome, classic type, 1 2023-07-07 criteria provided, single submitter clinical testing

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