ClinVar Miner

Submissions for variant NM_003322.6(TULP1):c.191-5C>T

dbSNP: rs2150928492
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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 RCV001440133 SCV001643037 likely benign not provided 2022-08-31 criteria provided, single submitter clinical testing

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