ClinVar Miner

Submissions for variant NM_000090.4(COL3A1):c.4182G>A (p.Gly1394=)

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Total submissions: 2
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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 RCV003479844 SCV004223700 likely benign not specified 2023-11-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003633728 SCV004520572 likely benign Ehlers-Danlos syndrome, type 4 2023-04-10 criteria provided, single submitter clinical testing

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