ClinVar Miner

Submissions for variant NM_001099274.3(TINF2):c.400-20_400-18dup

gnomAD frequency: 0.06483  dbSNP: rs58372573
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001520059 SCV001729067 benign Dyskeratosis congenita 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001676012 SCV001894586 benign not provided 2019-02-14 criteria provided, single submitter clinical testing

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