ClinVar Miner

Submissions for variant NM_015141.4(GPD1L):c.852+20C>T

gnomAD frequency: 0.00001  dbSNP: rs189819292
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000827845 SCV000969508 likely benign not provided 2018-03-26 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV002067467 SCV002402456 benign Brugada syndrome 2024-11-19 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005056614 SCV005725770 benign not specified 2024-11-26 criteria provided, single submitter clinical testing

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