ClinVar Miner

List of variants in gene APOB reported by Stanford Center for Inherited Cardiovascular Disease, Stanford University

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.11092A>G (p.Arg3698Gly)	rs757756141	0.00001
NM_000384.3(APOB):c.10580G>A (p.Arg3527Gln)
NM_000384.3(APOB):c.2096C>T (p.Pro699Leu)	rs776107514
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu)

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