ClinVar Miner

Submissions for variant NM_005562.3(LAMC2):c.2457-9C>T

dbSNP: rs774648846
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001488258 SCV001692765 likely benign not provided 2022-04-08 criteria provided, single submitter clinical testing

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