ClinVar Miner

Submissions for variant NM_021133.4(RNASEL):c.1385G>A (p.Arg462Gln)

gnomAD frequency: 0.28062  dbSNP: rs486907
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV003492293 SCV004232562 likely benign Hereditary cancer 2024-01-23 criteria provided, single submitter clinical testing
OMIM RCV004794338 SCV000034127 risk factor Prostate cancer susceptibility 2002-12-01 no assertion criteria provided literature only
Laboratory of Virology, Oncology, Biosciences and Environment, Faculty of Sciences and Techniques, Mohammedia- University Hassan II of Casablanca RCV002279713 SCV002567828 uncertain significance Prostate cancer, hereditary, 1 2022-08-17 no assertion criteria provided clinical testing

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