List of variants in gene APOB reported as likely 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: 84

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.7545C>T (p.Thr2515=)	rs693	0.38722
NM_000384.3(APOB):c.905-15C>G	rs72653061	0.00554
NM_000384.3(APOB):c.607A>G (p.Ile203Val)	rs72653059	0.00396
NM_000384.3(APOB):c.3383G>A (p.Arg1128His)	rs12713843	0.00356
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.11833A>G (p.Thr3945Ala)	rs1801698	0.00212
NM_000384.3(APOB):c.7615G>A (p.Val2539Ile)	rs148170480	0.00210
NM_000384.3(APOB):c.751G>A (p.Ala251Thr)	rs61741625	0.00190
NM_000384.3(APOB):c.905-16A>C	rs12720810	0.00172
NM_000384.3(APOB):c.11819C>T (p.Thr3940Met)	rs72654416	0.00161
NM_000384.3(APOB):c.2068-4T>A	rs41291161	0.00108
NM_000384.3(APOB):c.7612C>T (p.Leu2538=)	rs72653093	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.2310C>T (p.Val770=)	rs72653064	0.00036
NM_000384.3(APOB):c.8309C>T (p.Thr2770Ile)	rs138391809	0.00036
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.9639C>A (p.Asn3213Lys)	rs574725520	0.00025
NM_000384.3(APOB):c.11820G>A (p.Thr3940=)	rs72654417	0.00024
NM_000384.3(APOB):c.8994C>T (p.Gly2998=)	rs139332237	0.00024
NM_000384.3(APOB):c.3507T>C (p.Tyr1169=)	rs141763789	0.00021
NM_000384.3(APOB):c.11244G>A (p.Thr3748=)	rs72654406	0.00020
NM_000384.3(APOB):c.12016G>A (p.Val4006Ile)	rs183117027	0.00019
NM_000384.3(APOB):c.10385A>G (p.Tyr3462Cys)	rs200305144	0.00014
NM_000384.3(APOB):c.12088-14T>C	rs182329513	0.00011
NM_000384.3(APOB):c.4280G>A (p.Arg1427His)	rs145324793	0.00011
NM_000384.3(APOB):c.11911G>A (p.Glu3971Lys)	rs373477107	0.00009
NM_000384.3(APOB):c.10509G>A (p.Ser3503=)	rs769351301	0.00008
NM_000384.3(APOB):c.13288T>A (p.Ser4430Thr)	rs72654426	0.00008
NM_000384.3(APOB):c.2841C>T (p.Thr947=)	rs72653070	0.00008
NM_000384.3(APOB):c.12736T>G (p.Phe4246Val)	rs200260789	0.00007
NM_000384.3(APOB):c.7998A>G (p.Val2666=)	rs1042006	0.00007
NM_000384.3(APOB):c.5183A>G (p.Asn1728Ser)	rs186346145	0.00006
NM_000384.3(APOB):c.10371C>T (p.Ser3457=)	rs139891446	0.00005
NM_000384.3(APOB):c.7575A>G (p.Gln2525=)	rs377302171	0.00005
NM_000384.3(APOB):c.10739A>G (p.Asn3580Ser)	rs762028704	0.00004
NM_000384.3(APOB):c.11319G>A (p.Lys3773=)	rs780811733	0.00004
NM_000384.3(APOB):c.10344C>T (p.Thr3448=)	rs13306193	0.00003
NM_000384.3(APOB):c.12024C>T (p.Thr4008=)	rs145269223	0.00002
NM_000384.3(APOB):c.8469T>C (p.Ala2823=)	rs531216195	0.00002
NM_000384.3(APOB):c.11585T>C (p.Ile3862Thr)	rs772015796	0.00001
NM_000384.3(APOB):c.12636T>C (p.Thr4212=)	rs772812955	0.00001
NM_000384.3(APOB):c.13154G>A (p.Arg4385His)	rs533755016	0.00001
NM_000384.3(APOB):c.1395C>T (p.Asp465=)	rs757609661	0.00001
NM_000384.3(APOB):c.2437-17C>T	rs764415047	0.00001
NM_000384.3(APOB):c.7283A>G (p.Lys2428Arg)	rs1369533953	0.00001
NM_000384.3(APOB):c.8530C>T (p.Leu2844=)	rs1553383318	0.00001
NM_000384.3(APOB):c.9445G>A (p.Asp3149Asn)	rs759354804	0.00001
NM_000384.3(APOB):c.10061C>G (p.Ala3354Gly)
NM_000384.3(APOB):c.10323G>A (p.Lys3441=)	rs1663144038
NM_000384.3(APOB):c.10326A>G (p.Gln3442=)
NM_000384.3(APOB):c.10413T>C (p.Ser3471=)
NM_000384.3(APOB):c.10520G>C (p.Arg3507Pro)	rs201156840
NM_000384.3(APOB):c.10581G>A (p.Arg3527=)	rs1663135017
NM_000384.3(APOB):c.10780T>C (p.Trp3594Arg)
NM_000384.3(APOB):c.10913G>A (p.Arg3638Gln)
NM_000384.3(APOB):c.11442C>G (p.Thr3814=)	rs72654408
NM_000384.3(APOB):c.12541G>A (p.Glu4181Lys)
NM_000384.3(APOB):c.13013G>A (p.Ser4338Asn)
NM_000384.3(APOB):c.13368C>A (p.Thr4456=)	rs1553382258
NM_000384.3(APOB):c.13441G>A (p.Ala4481Thr)
NM_000384.3(APOB):c.1594C>T (p.Arg532Trp)
NM_000384.3(APOB):c.1853C>T (p.Ala618Val)
NM_000384.3(APOB):c.1903C>A (p.Arg635=)	rs548108916
NM_000384.3(APOB):c.293C>T (p.Thr98Ile)
NM_000384.3(APOB):c.3122-6G>A	rs72653071
NM_000384.3(APOB):c.3337G>C (p.Asp1113His)
NM_000384.3(APOB):c.3491G>A (p.Arg1164Lys)	rs759845943
NM_000384.3(APOB):c.3508+17_3508+18del	rs1553384473
NM_000384.3(APOB):c.3561A>G (p.Lys1187=)	rs2103362720
NM_000384.3(APOB):c.4140A>G (p.Thr1380=)	rs781016611
NM_000384.3(APOB):c.5066G>A (p.Arg1689His)
NM_000384.3(APOB):c.5741A>G (p.Asn1914Ser)
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.7930A>C (p.Arg2644=)	rs1553383425
NM_000384.3(APOB):c.8216C>T (p.Pro2739Leu)
NM_000384.3(APOB):c.9378A>G (p.Leu3126=)	rs760776177

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