ClinVar Miner

Submissions for variant NM_001283009.2(RTEL1):c.1626G>A (p.Gly542=)

gnomAD frequency: 0.00009  dbSNP: rs140629792
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000880775 SCV001023897 likely benign Dyskeratosis congenita, autosomal recessive 5; Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3 2024-12-23 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002255566 SCV002535296 likely benign Dyskeratosis congenita 2020-09-30 criteria provided, single submitter curation
Ambry Genetics RCV002399976 SCV002714243 likely benign Inborn genetic diseases 2022-02-14 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Natera, Inc. RCV001277128 SCV001463956 likely benign Dyskeratosis congenita, autosomal dominant 1 2020-04-30 no assertion criteria provided clinical testing

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