ClinVar Miner

Submissions for variant NM_016816.4(OAS1):c.884+10C>T

gnomAD frequency: 0.00249  dbSNP: rs143035510
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001512698 SCV001720157 benign not provided 2024-01-10 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003921090 SCV004742692 likely benign OAS1-related disorder 2024-02-20 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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