ClinVar Miner

Submissions for variant NM_000094.4(COL7A1):c.6715-18C>T

gnomAD frequency: 0.01922  dbSNP: rs13325221
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001509646 SCV001716473 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001509646 SCV001839938 benign not provided 2018-07-05 criteria provided, single submitter clinical testing

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