List of variants in gene APOB reported as benign for not specified

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: 93

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.6937A>G (p.Ile2313Val)	rs584542	0.98330
NM_000384.3(APOB):c.7545C>T (p.Thr2515=)	rs693	0.38722
NM_000384.3(APOB):c.6936C>T (p.Asp2312=)	rs1041968	0.38695
NM_000384.3(APOB):c.2706C>T (p.Asn902=)	rs1801700	0.03627
NM_000384.3(APOB):c.11904-7C>T	rs12720851	0.03622
NM_000384.3(APOB):c.538-9C>T	rs1800478	0.03349
NM_000384.3(APOB):c.10737C>T (p.Thr3579=)	rs12713554	0.02896
NM_000384.3(APOB):c.8148C>T (p.Ile2716=)	rs6413458	0.02288
NM_000384.3(APOB):c.10701G>A (p.Thr3567=)	rs12713558	0.02176
NM_000384.3(APOB):c.9004C>T (p.Leu3002=)	rs12713600	0.01938
NM_000384.3(APOB):c.4365C>T (p.Phe1455=)	rs12720847	0.01812
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.2244+3G>A	rs12714189	0.00920
NM_000384.3(APOB):c.2604+15G>C	rs72653066	0.00842
NM_000384.3(APOB):c.10131G>A (p.Leu3377=)	rs1799812	0.00564
NM_000384.3(APOB):c.905-15C>G	rs72653061	0.00554
NM_000384.3(APOB):c.12794T>C (p.Val4265Ala)	rs61743502	0.00516
NM_000384.3(APOB):c.8353A>C (p.Asn2785His)	rs2163204	0.00306
NM_000384.3(APOB):c.7696G>A (p.Glu2566Lys)	rs1801696	0.00305
NM_000384.3(APOB):c.8462C>T (p.Pro2821Leu)	rs72653095	0.00267
NM_000384.3(APOB):c.13369G>A (p.Asp4457Asn)	rs183812948	0.00250
NM_000384.3(APOB):c.4825T>C (p.Leu1609=)	rs72653083	0.00242
NM_000384.3(APOB):c.3843C>T (p.Ser1281=)	rs72653079	0.00240
NM_000384.3(APOB):c.3426G>A (p.Ser1142=)	rs142448733	0.00177
NM_000384.3(APOB):c.9105T>C (p.Asn3035=)	rs147510760	0.00166
NM_000384.3(APOB):c.3279C>G (p.Thr1093=)	rs72653075	0.00163
NM_000384.3(APOB):c.9294C>T (p.Tyr3098=)	rs145777339	0.00139
NM_000384.3(APOB):c.12699G>A (p.Ser4233=)	rs56675344	0.00136
NM_000384.3(APOB):c.2068-4T>A	rs41291161	0.00108
NM_000384.3(APOB):c.4838G>C (p.Ser1613Thr)	rs61742247	0.00093
NM_000384.3(APOB):c.4163G>A (p.Arg1388His)	rs13306187	0.00088
NM_000384.3(APOB):c.9477G>A (p.Lys3159=)	rs13306196	0.00073
NM_000384.3(APOB):c.7152T>C (p.Val2384=)	rs72653090	0.00041
NM_000384.3(APOB):c.9855C>T (p.Ile3285=)	rs72654403	0.00041
NM_000384.3(APOB):c.12252T>C (p.Tyr4084=)	rs138157751	0.00034
NM_000384.3(APOB):c.2853G>A (p.Glu951=)	rs151193347	0.00031
NM_000384.3(APOB):c.2817-19T>G	rs72653069	0.00025
NM_000384.3(APOB):c.8550T>G (p.Ile2850Met)	rs148498577	0.00024
NM_000384.3(APOB):c.7863A>C (p.Leu2621=)	rs138497378	0.00022
NM_000384.3(APOB):c.3507T>C (p.Tyr1169=)	rs141763789	0.00021
NM_000384.3(APOB):c.6018C>T (p.Gly2006=)	rs368422207	0.00016
NM_000384.3(APOB):c.12051C>T (p.Asp4017=)	rs12713501	0.00013
NM_000384.3(APOB):c.10575C>T (p.Ser3525=)	rs142573551	0.00010
NM_000384.3(APOB):c.2823A>G (p.Thr941=)	rs200868559	0.00008
NM_000384.3(APOB):c.3034G>A (p.Glu1012Lys)	rs575505383	0.00003
NM_000384.3(APOB):c.6513A>G (p.Leu2171=)	rs547853968	0.00003
NM_000384.3(APOB):c.1595G>A (p.Arg532Gln)	rs753831464	0.00002
NM_000384.3(APOB):c.8469T>C (p.Ala2823=)	rs531216195	0.00002
NM_000384.3(APOB):c.10657G>A (p.Glu3553Lys)	rs763118165	0.00001
NM_000384.3(APOB):c.10734C>T (p.Phe3578=)	rs773361538	0.00001
NM_000384.3(APOB):c.11826C>T (p.Ala3942=)	rs775360043	0.00001
NM_000384.3(APOB):c.11854C>T (p.Arg3952Cys)	rs535121944	0.00001
NM_000384.3(APOB):c.13154G>A (p.Arg4385His)	rs533755016	0.00001
NM_000384.3(APOB):c.13160A>T (p.Glu4387Val)	rs150412734	0.00001
NM_000384.3(APOB):c.10294C>G (p.Gln3432Glu)
NM_000384.3(APOB):c.10520G>C (p.Arg3507Pro)	rs201156840
NM_000384.3(APOB):c.10740C>T (p.Asn3580=)	rs150312765
NM_000384.3(APOB):c.10780T>C (p.Trp3594Arg)
NM_000384.3(APOB):c.10913G>A (p.Arg3638Gln)
NM_000384.3(APOB):c.11401T>A (p.Ser3801Thr)
NM_000384.3(APOB):c.11477C>T (p.Thr3826Met)
NM_000384.3(APOB):c.11761G>A (p.Val3921Ile)
NM_000384.3(APOB):c.1223T>C (p.Ile408Thr)
NM_000384.3(APOB):c.12382G>A (p.Val4128Met)
NM_000384.3(APOB):c.12541G>A (p.Glu4181Lys)
NM_000384.3(APOB):c.12697T>A (p.Ser4233Thr)
NM_000384.3(APOB):c.12809G>C (p.Arg4270Thr)
NM_000384.3(APOB):c.12940A>G (p.Ile4314Val)
NM_000384.3(APOB):c.13013G>A (p.Ser4338Asn)
NM_000384.3(APOB):c.13441G>A (p.Ala4481Thr)
NM_000384.3(APOB):c.13451C>T (p.Thr4484Met)
NM_000384.3(APOB):c.1594C>T (p.Arg532Trp)
NM_000384.3(APOB):c.1853C>T (p.Ala618Val)
NM_000384.3(APOB):c.2188G>A (p.Val730Ile)
NM_000384.3(APOB):c.2222C>A (p.Thr741Asn)
NM_000384.3(APOB):c.293C>T (p.Thr98Ile)
NM_000384.3(APOB):c.3337G>C (p.Asp1113His)
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser)
NM_000384.3(APOB):c.3634C>A (p.Leu1212Met)
NM_000384.3(APOB):c.4265= (p.Cys1422=)
NM_000384.3(APOB):c.433C>T (p.Pro145Ser)
NM_000384.3(APOB):c.5741A>G (p.Asn1914Ser)
NM_000384.3(APOB):c.5768A>G (p.His1923Arg)
NM_000384.3(APOB):c.6636TGA[1] (p.Asp2213del)	rs541497967
NM_000384.3(APOB):c.6895G>C (p.Asp2299His)
NM_000384.3(APOB):c.6936_6937inv (p.Ile2313Val)
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr)
NM_000384.3(APOB):c.7367C>A (p.Ala2456Asp)
NM_000384.3(APOB):c.8216C>T (p.Pro2739Leu)
NM_000384.3(APOB):c.900T>C (p.Gly300=)	rs549628916
NM_000384.3(APOB):c.9835A>G (p.Ser3279Gly)
NM_000384.3(APOB):c.9880T>C (p.Ser3294Pro)

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