ClinVar Miner

Submissions for variant NM_000237.3(LPL):c.542-8C>T

gnomAD frequency: 0.00059  dbSNP: rs201634558
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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 RCV000931755 SCV001077426 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003323762 SCV004030102 uncertain significance not specified 2023-07-17 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832118 SCV002083206 likely benign Hyperlipoproteinemia, type I 2019-10-24 no assertion criteria provided clinical testing

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