ClinVar Miner

Submissions for variant NM_000094.4(COL7A1):c.5737-17G>T

gnomAD frequency: 0.00117  dbSNP: rs150337561
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
Invitae RCV001520412 SCV001729506 benign not provided 2024-01-31 criteria provided, single submitter clinical testing

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