ClinVar Miner

Submissions for variant NM_001099274.3(TINF2):c.400-11C>G

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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 RCV003646186 SCV004401611 likely benign Dyskeratosis congenita 2023-01-21 criteria provided, single submitter clinical testing

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