ClinVar Miner

Submissions for variant NM_015559.3(SETBP1):c.161G>T (p.Arg54Leu)

dbSNP: rs140717709
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001884421 SCV002150999 benign not provided 2023-10-24 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV001884421 SCV004224482 uncertain significance not provided 2022-09-28 criteria provided, single submitter clinical testing BP4

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