ClinVar Miner

Submissions for variant NM_000527.5(LDLR):c.694+7G>C

dbSNP: rs1600711821
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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 RCV001480329 SCV001684645 likely benign Familial hypercholesterolemia 2020-09-16 criteria provided, single submitter clinical testing

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