ClinVar Miner

Submissions for variant NM_000384.3(APOB):c.237+92G>T

dbSNP: rs661665
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001553837 SCV001774910 benign Hypercholesterolemia, autosomal dominant, type B 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001553838 SCV001774911 benign Familial hypobetalipoproteinemia 1 2021-07-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710313 SCV005245261 benign not provided criteria provided, single submitter not provided

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