ClinVar Miner

Submissions for variant NM_198253.3(TERT):c.3324G>C (p.Pro1108=)

dbSNP: rs35033501
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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 RCV001437746 SCV001640609 likely benign Interstitial lung disease 2; Dyskeratosis congenita, autosomal dominant 2 2021-01-16 criteria provided, single submitter clinical testing

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