ClinVar Miner

Submissions for variant NM_000384.3(APOB):c.354C>T (p.Asn118=)

dbSNP: rs781633079
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002068261 SCV002328723 likely benign Hypercholesterolemia, autosomal dominant, type B; Familial hypobetalipoproteinemia 1 2021-07-20 criteria provided, single submitter clinical testing

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