ClinVar Miner

Submissions for variant NM_198253.3(TERT):c.1574-3235G>T

gnomAD frequency: 0.28965  dbSNP: rs7705526
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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 RCV001513602 SCV001721245 benign Interstitial lung disease 2; Dyskeratosis congenita, autosomal dominant 2 2020-12-04 criteria provided, single submitter clinical testing

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