ClinVar Miner

Submissions for variant NM_018013.4(SOBP):c.2232GCC[8] (p.Pro751dup)

dbSNP: rs541688197
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000889582 SCV001033276 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001818654 SCV002069788 benign not specified 2019-06-07 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003940642 SCV004747829 likely benign SOBP-related disorder 2019-10-01 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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