ClinVar Miner

Submissions for variant NM_000384.3(APOB):c.10575C>T (p.Ser3525=) (rs142573551)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000776252 SCV000911504 likely benign Familial hypercholesterolemias 2018-04-12 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000392217 SCV000426987 uncertain significance Familial hypercholesterolemia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000308927 SCV000426988 uncertain significance Familial hypobetalipoproteinemia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000467612 SCV000554827 likely benign Hypercholesterolemia, autosomal dominant, type B; Hypobetalipoproteinemia, familial, 1 2016-07-31 criteria provided, single submitter clinical testing

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