ClinVar Miner

Submissions for variant NM_000094.4(COL7A1):c.4342-13G>A

gnomAD frequency: 0.00001  dbSNP: rs942776933
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
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 RCV003155704 SCV003844527 uncertain significance not specified 2023-02-11 criteria provided, single submitter clinical testing

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