ClinVar Miner

Submissions for variant NM_001099274.3(TINF2):c.400-6C>T

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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 RCV003041511 SCV003321675 likely benign Dyskeratosis congenita 2022-02-27 criteria provided, single submitter clinical testing

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