ClinVar Miner

List of variants in gene APOB reported as likely benign by CSER _CC_NCGL, University of Washington

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.1648G>C (p.Asp550His) rs145862664 0.00006
NM_000384.3(APOB):c.11362G>A (p.Glu3788Lys) rs13306191 0.00005

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