ClinVar Miner

Submissions for variant NM_198253.3(TERT):c.2844-12C>A

dbSNP: rs199765802
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001817430 SCV002068249 uncertain significance not specified 2018-01-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002542532 SCV002394360 likely benign Dyskeratosis congenita, autosomal dominant 2; Idiopathic Pulmonary Fibrosis 2024-01-21 criteria provided, single submitter clinical testing

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