ClinVar Miner

Submissions for variant NM_000094.4(COL7A1):c.4819-19C>T

gnomAD frequency: 0.00011  dbSNP: rs371699045
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002154884 SCV002334734 benign not provided 2024-09-02 criteria provided, single submitter clinical testing

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