ClinVar Miner

Submissions for variant NM_003383.5(VLDLR):c.397A>C (p.Arg133=)

gnomAD frequency: 0.00001  dbSNP: rs1306172005
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000974221 SCV001122036 likely benign not provided 2023-11-11 criteria provided, single submitter clinical testing

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