ClinVar Miner

List of variants in gene combination APOB, APOB3'MAR reported as pathogenic for Hypercholesterolemia, autosomal dominant, type B; Familial hypobetalipoproteinemia 1

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Total variants: 1
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HGVS dbSNP gnomAD frequency
NC_000002.12:g.(?_21001710)_(21035728_?)del

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