ClinVar Miner

Submissions for variant NM_000527.5(LDLR):c.1060+10G>T

dbSNP: rs12710260
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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 RCV001458169 SCV001661984 likely benign Familial hypercholesterolemia 2023-11-24 criteria provided, single submitter clinical testing

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