ClinVar Miner

Submissions for variant NM_000094.4(COL7A1):c.8407+10G>T

dbSNP: rs754593655
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000979133 SCV001127072 likely benign not provided 2024-01-22 criteria provided, single submitter clinical testing
Natera, Inc. RCV001275470 SCV001460634 uncertain significance Epidermolysis bullosa dystrophica 2020-03-10 no assertion criteria provided clinical testing

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