ClinVar Miner

Submissions for variant NM_015627.3(LDLRAP1):c.27G>C (p.Arg9=)

dbSNP: rs1340216590
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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 RCV001463868 SCV001667818 likely benign Hypercholesterolemia, familial, 4 2023-12-06 criteria provided, single submitter clinical testing

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