List of variants in gene APOB reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.13013G>A (p.Ser4338Asn)	rs1042034	0.76948
NM_000384.3(APOB):c.1853C>T (p.Ala618Val)	rs679899	0.40054
NM_000384.3(APOB):c.7545C>T (p.Thr2515=)	rs693	0.38001
NM_000384.3(APOB):c.12541G>A (p.Glu4181Lys)	rs1042031	0.16481
NM_000384.3(APOB):c.10913G>A (p.Arg3638Gln)	rs1801701	0.06584
NM_000384.3(APOB):c.12809G>C (p.Arg4270Thr)	rs1801702	0.05420
NM_000384.3(APOB):c.11904-7C>T	rs12720851	0.03622
NM_000384.3(APOB):c.2706C>T (p.Asn902=)	rs1801700	0.03503
NM_000384.3(APOB):c.13451C>T (p.Thr4484Met)	rs12713450	0.03392
NM_000384.3(APOB):c.5768A>G (p.His1923Arg)	rs533617	0.02869
NM_000384.3(APOB):c.10737C>T (p.Thr3579=)	rs12713554	0.02731
NM_000384.3(APOB):c.2188G>A (p.Val730Ile)	rs12691202	0.02673
NM_000384.3(APOB):c.5741A>G (p.Asn1914Ser)	rs1801699	0.01706
NM_000384.3(APOB):c.11808C>T (p.Ile3936=)	rs12720852	0.01624
NM_000384.3(APOB):c.3509-10G>A	rs12720770	0.01624
NM_000384.3(APOB):c.9880T>C (p.Ser3294Pro)	rs12720855	0.01525
NM_000384.3(APOB):c.7367C>A (p.Ala2456Asp)	rs12713675	0.01524
NM_000384.3(APOB):c.12697T>A (p.Ser4233Thr)	rs61743299	0.01522
NM_000384.3(APOB):c.2604+15G>C	rs72653066	0.00842
NM_000384.3(APOB):c.9835A>G (p.Ser3279Gly)	rs12720854	0.00761
NM_000384.3(APOB):c.1785C>G (p.Ser595=)	rs139864087	0.00247
NM_000384.3(APOB):c.11761G>A (p.Val3921Ile)	rs72654409	0.00234
NM_000384.3(APOB):c.7242A>C (p.Glu2414Asp)	rs72653091	0.00212
NM_000384.3(APOB):c.12766G>A (p.Glu4256Lys)	rs61743313	0.00198
NM_000384.3(APOB):c.6513A>G (p.Leu2171=)	rs547853968	0.00036
NM_000384.3(APOB):c.8877G>A (p.Leu2959=)	rs765899256	0.00012
NM_000384.3(APOB):c.6936_6937inv (p.Ile2313Val)
NM_000384.3(APOB):c.8216C>T (p.Pro2739Leu)	rs676210

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