ClinVar Miner

Submissions for variant NM_003383.5(VLDLR):c.75C>T (p.Thr25=)

gnomAD frequency: 0.00112  dbSNP: rs532555108
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000194158 SCV000249389 likely benign not specified 2015-07-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000904884 SCV001049437 benign not provided 2024-10-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000904884 SCV005225288 likely benign not provided criteria provided, single submitter not provided

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