ClinVar Miner

Submissions for variant NM_015627.3(LDLRAP1):c.54C>T (p.Ala18=)

dbSNP: rs2124633760
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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 RCV002217345 SCV002365777 likely benign Hypercholesterolemia, familial, 4 2021-05-07 criteria provided, single submitter clinical testing

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