ClinVar Miner

Submissions for variant NM_015627.3(LDLRAP1):c.24G>C (p.Gly8=)

dbSNP: rs1334466061
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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 RCV001495940 SCV001700630 likely benign Hypercholesterolemia, familial, 4 2023-01-27 criteria provided, single submitter clinical testing

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