ClinVar Miner

Submissions for variant NM_000255.4(MMUT):c.1444+7T>C

dbSNP: rs1767475370
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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 RCV001411427 SCV001613490 likely benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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