ClinVar Miner

Submissions for variant NM_015627.3(LDLRAP1):c.69G>T (p.Gly23=)

gnomAD frequency: 0.00001  dbSNP: rs868048475
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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 RCV001503443 SCV001708298 likely benign Hypercholesterolemia, familial, 4 2023-11-13 criteria provided, single submitter clinical testing

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