ClinVar Miner

Submissions for variant NM_001099274.3(TINF2):c.27C>T (p.Pro9=)

dbSNP: rs754494652
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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 RCV003018810 SCV003313759 likely benign Dyskeratosis congenita 2022-09-01 criteria provided, single submitter clinical testing

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