ClinVar Miner

Submissions for variant NM_003176.4(SYCP1):c.260A>G (p.Tyr87Cys)

gnomAD frequency: 0.00273  dbSNP: rs146221635
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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 RCV000970056 SCV001117612 likely benign not provided 2018-07-16 criteria provided, single submitter clinical testing
Brain Center Rudolf Magnus, University Medical Center Utrecht RCV001730743 SCV001980676 uncertain significance Mycotic Aneurysm, Intracranial 2021-10-08 criteria provided, single submitter research

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