ClinVar Miner

Submissions for variant NM_000384.3(APOB):c.2823A>G (p.Thr941=) (rs200868559)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000287931 SCV000427128 likely benign Familial hypobetalipoproteinemia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000345190 SCV000427129 likely benign Familial hypercholesterolemia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000467370 SCV000554830 benign not provided 2018-12-20 criteria provided, single submitter clinical testing
Color RCV000771125 SCV000902876 benign Familial hypercholesterolemias 2017-11-23 criteria provided, single submitter clinical testing

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