ClinVar Miner

Submissions for variant NM_003383.5(VLDLR):c.1485-12A>G

gnomAD frequency: 0.00163  dbSNP: rs146156696
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000436321 SCV000521474 likely benign not provided 2020-10-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000436321 SCV002408767 benign not provided 2024-12-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000436321 SCV005225297 likely benign not provided criteria provided, single submitter not provided

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