ClinVar Miner

Submissions for variant NM_001283009.2(RTEL1):c.2856C>T (p.Phe952=)

dbSNP: rs1041575386
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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 RCV001424989 SCV001627599 likely benign Dyskeratosis congenita, autosomal recessive 5; Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3 2023-06-10 criteria provided, single submitter clinical testing

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