ClinVar Miner

Submissions for variant NM_001099274.3(TINF2):c.1269C>A (p.Pro423=)

dbSNP: rs777077289
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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 RCV002162723 SCV002420742 likely benign Dyskeratosis congenita 2021-10-02 criteria provided, single submitter clinical testing

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