ClinVar Miner

List of variants in gene APOB reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 139
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.11257T>C (p.Phe3753Leu) rs61741974 0.00213
NM_000384.3(APOB):c.3712C>A (p.Leu1238Ile) rs72653078 0.00091
NM_000384.3(APOB):c.4178C>T (p.Ala1393Val) rs143282164 0.00073
NM_000384.3(APOB):c.3740A>G (p.Tyr1247Cys) rs61741164 0.00071
NM_000384.3(APOB):c.4187T>C (p.Val1396Ala) rs144034290 0.00036
NM_000384.3(APOB):c.11720A>G (p.Asp3907Gly) rs61746686 0.00034
NM_000384.3(APOB):c.2411G>A (p.Arg804His) rs148190577 0.00031
NM_000384.3(APOB):c.914A>G (p.Lys305Arg) rs199937544 0.00029
NM_000384.3(APOB):c.9883T>C (p.Tyr3295His) rs186299244 0.00027
NM_000384.3(APOB):c.5599C>T (p.Arg1867Trp) rs200583769 0.00024
NM_000384.3(APOB):c.8550T>G (p.Ile2850Met) rs148498577 0.00024
NM_000384.3(APOB):c.10708C>T (p.His3570Tyr) rs201736972 0.00021
NM_000384.3(APOB):c.3724T>A (p.Ser1242Thr) rs200261177 0.00020
NM_000384.3(APOB):c.13444A>G (p.Ile4482Val) rs142702699 0.00019
NM_000384.3(APOB):c.4532C>T (p.Thr1511Ile) rs146247063 0.00019
NM_000384.3(APOB):c.3200C>T (p.Pro1067Leu) rs146133928 0.00017
NM_000384.3(APOB):c.6969T>A (p.Asn2323Lys) rs138118085 0.00016
NM_000384.3(APOB):c.11542G>A (p.Ala3848Thr) rs61743512 0.00012
NM_000384.3(APOB):c.11569G>A (p.Val3857Met) rs145655926 0.00012
NM_000384.3(APOB):c.288G>T (p.Gln96His) rs186544754 0.00012
NM_000384.3(APOB):c.2204T>A (p.Val735Glu) rs199872875 0.00011
NM_000384.3(APOB):c.574G>A (p.Val192Ile) rs200662943 0.00011
NM_000384.3(APOB):c.11965C>T (p.Arg3989Cys) rs150713761 0.00010
NM_000384.3(APOB):c.1316G>A (p.Arg439Gln) rs61742990 0.00010
NM_000384.3(APOB):c.11233G>A (p.Val3745Ile) rs147564959 0.00009
NM_000384.3(APOB):c.5044A>G (p.Met1682Val) rs140858817 0.00009
NM_000384.3(APOB):c.11966G>A (p.Arg3989His) rs148197354 0.00008
NM_000384.3(APOB):c.13175G>A (p.Ser4392Asn) rs777718986 0.00008
NM_000384.3(APOB):c.13288T>A (p.Ser4430Thr) rs72654426 0.00008
NM_000384.3(APOB):c.2312C>T (p.Pro771Leu) rs200524554 0.00007
NM_000384.3(APOB):c.2938G>A (p.Ala980Thr) rs369310292 0.00007
NM_000384.3(APOB):c.9491C>T (p.Thr3164Met) rs143269114 0.00007
NM_000384.3(APOB):c.10267G>A (p.Val3423Met) rs199689957 0.00006
NM_000384.3(APOB):c.5863G>A (p.Val1955Met) rs368970025 0.00006
NM_000384.3(APOB):c.8134C>T (p.Arg2712Cys) rs372245645 0.00006
NM_000384.3(APOB):c.8198T>C (p.Val2733Ala) rs771792572 0.00006
NM_000384.3(APOB):c.9407G>A (p.Arg3136His) rs199590149 0.00006
NM_000384.3(APOB):c.6223G>A (p.Glu2075Lys) rs377429190 0.00005
NM_000384.3(APOB):c.7057C>A (p.Gln2353Lys) rs758067709 0.00005
NM_000384.3(APOB):c.7655A>G (p.Asp2552Gly) rs779100523 0.00005
NM_000384.3(APOB):c.12136C>T (p.Arg4046Trp) rs200222843 0.00004
NM_000384.3(APOB):c.12695A>G (p.Tyr4232Cys) rs767269509 0.00004
NM_000384.3(APOB):c.1400C>G (p.Ala467Gly) rs376602710 0.00004
NM_000384.3(APOB):c.1472T>C (p.Val491Ala) rs996700659 0.00004
NM_000384.3(APOB):c.1753C>A (p.Gln585Lys) rs140101603 0.00004
NM_000384.3(APOB):c.3607A>G (p.Ser1203Gly) rs78875649 0.00004
NM_000384.3(APOB):c.721A>T (p.Ser241Cys) rs758838678 0.00004
NM_000384.3(APOB):c.13448C>T (p.Ala4483Val) rs147416761 0.00003
NM_000384.3(APOB):c.4143C>A (p.Asp1381Glu) rs754597311 0.00003
NM_000384.3(APOB):c.598G>A (p.Ala200Thr) rs763878189 0.00003
NM_000384.3(APOB):c.5991T>A (p.Asp1997Glu) rs768045701 0.00003
NM_000384.3(APOB):c.6659T>C (p.Val2220Ala) rs374736992 0.00003
NM_000384.3(APOB):c.7565G>A (p.Arg2522Gln) rs781243278 0.00003
NM_000384.3(APOB):c.7823A>C (p.Gln2608Pro) rs767180578 0.00003
NM_000384.3(APOB):c.889C>T (p.Arg297Cys) rs766376456 0.00003
NM_000384.3(APOB):c.10037G>T (p.Ser3346Ile) rs373190270 0.00002
NM_000384.3(APOB):c.5065C>T (p.Arg1689Cys) rs780820172 0.00002
NM_000384.3(APOB):c.5459A>C (p.Lys1820Thr) rs180874451 0.00002
NM_000384.3(APOB):c.6001A>G (p.Thr2001Ala) rs140327327 0.00002
NM_000384.3(APOB):c.7559G>A (p.Arg2520Gln) rs199852015 0.00002
NM_000384.3(APOB):c.9095C>A (p.Thr3032Asn) rs754332101 0.00002
NM_000384.3(APOB):c.9721G>A (p.Glu3241Lys) rs139245086 0.00002
NM_000384.3(APOB):c.10679A>G (p.Tyr3560Cys) rs745721296 0.00001
NM_000384.3(APOB):c.11162T>C (p.Ile3721Thr) rs202213088 0.00001
NM_000384.3(APOB):c.11356C>T (p.Leu3786Phe) rs571485213 0.00001
NM_000384.3(APOB):c.11681A>T (p.Tyr3894Phe) rs775669767 0.00001
NM_000384.3(APOB):c.12343G>T (p.Val4115Phe) rs765681925 0.00001
NM_000384.3(APOB):c.1302G>T (p.Arg434Ser) rs1484695395 0.00001
NM_000384.3(APOB):c.13422G>C (p.Gln4474His) rs146661220 0.00001
NM_000384.3(APOB):c.1469G>A (p.Arg490Gln) rs746365267 0.00001
NM_000384.3(APOB):c.1511C>G (p.Pro504Arg) rs1053904822 0.00001
NM_000384.3(APOB):c.2398C>A (p.Leu800Met) rs183950016 0.00001
NM_000384.3(APOB):c.3283G>A (p.Asp1095Asn) rs1377332778 0.00001
NM_000384.3(APOB):c.3829C>T (p.Leu1277Phe) rs544542990 0.00001
NM_000384.3(APOB):c.6572T>C (p.Leu2191Ser) rs766444813 0.00001
NM_000384.3(APOB):c.676G>A (p.Ala226Thr) rs1163833540 0.00001
NM_000384.3(APOB):c.7409T>C (p.Leu2470Ser) rs746574955 0.00001
NM_000384.3(APOB):c.8227C>G (p.Leu2743Val) rs777302365 0.00001
NM_000384.3(APOB):c.8394G>T (p.Glu2798Asp) rs760517113 0.00001
NM_000384.3(APOB):c.9143C>A (p.Ala3048Glu) rs1423272093 0.00001
NM_000384.3(APOB):c.10031A>C (p.Lys3344Thr) rs2103352338
NM_000384.3(APOB):c.10129C>G (p.Leu3377Val)
NM_000384.3(APOB):c.10324C>A (p.Gln3442Lys) rs1663143963
NM_000384.3(APOB):c.10360G>A (p.Val3454Ile)
NM_000384.3(APOB):c.10481C>T (p.Ser3494Leu)
NM_000384.3(APOB):c.10511T>C (p.Val3504Ala) rs1663137529
NM_000384.3(APOB):c.10672C>T (p.Arg3558Cys)
NM_000384.3(APOB):c.10740C>G (p.Asn3580Lys) rs150312765
NM_000384.3(APOB):c.10778C>T (p.Pro3593Leu) rs1553382921
NM_000384.3(APOB):c.10810G>T (p.Ala3604Ser)
NM_000384.3(APOB):c.11596T>C (p.Ser3866Pro) rs769732943
NM_000384.3(APOB):c.11770C>G (p.Leu3924Val)
NM_000384.3(APOB):c.11944G>A (p.Ala3982Thr) rs1291270341
NM_000384.3(APOB):c.12945A>C (p.Lys4315Asn) rs1428180002
NM_000384.3(APOB):c.13477CAG[1] (p.Gln4494del) rs562574661
NM_000384.3(APOB):c.13573A>T (p.Ile4525Phe) rs1396812245
NM_000384.3(APOB):c.1568T>C (p.Ile523Thr) rs781234577
NM_000384.3(APOB):c.1777G>C (p.Val593Leu) rs781228974
NM_000384.3(APOB):c.2450T>C (p.Ile817Thr) rs1324775693
NM_000384.3(APOB):c.253C>T (p.Pro85Ser) rs1664121265
NM_000384.3(APOB):c.2726C>T (p.Ser909Leu)
NM_000384.3(APOB):c.2826A>T (p.Leu942Phe)
NM_000384.3(APOB):c.2863C>T (p.Pro955Ser)
NM_000384.3(APOB):c.2968G>A (p.Ala990Thr)
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu)
NM_000384.3(APOB):c.307T>C (p.Tyr103His)
NM_000384.3(APOB):c.3397G>T (p.Ala1133Ser)
NM_000384.3(APOB):c.3490A>G (p.Arg1164Gly)
NM_000384.3(APOB):c.3491G>C (p.Arg1164Thr)
NM_000384.3(APOB):c.3709T>G (p.Trp1237Gly) rs935161396
NM_000384.3(APOB):c.3863C>T (p.Thr1288Ile) rs745401772
NM_000384.3(APOB):c.400G>A (p.Ala134Thr) rs368321279
NM_000384.3(APOB):c.4180G>A (p.Asp1394Asn)
NM_000384.3(APOB):c.4658G>A (p.Gly1553Asp) rs1663344384
NM_000384.3(APOB):c.4676C>T (p.Ala1559Val) rs549741449
NM_000384.3(APOB):c.4688A>G (p.Tyr1563Cys)
NM_000384.3(APOB):c.4754A>T (p.Asn1585Ile) rs549983245
NM_000384.3(APOB):c.4796G>T (p.Arg1599Leu) rs746414462
NM_000384.3(APOB):c.5636T>G (p.Ile1879Ser) rs963000267
NM_000384.3(APOB):c.5848A>G (p.Thr1950Ala) rs1663301144
NM_000384.3(APOB):c.6227C>T (p.Thr2076Ile)
NM_000384.3(APOB):c.6443A>T (p.Lys2148Met) rs1011350296
NM_000384.3(APOB):c.6548A>G (p.Gln2183Arg)
NM_000384.3(APOB):c.6961G>C (p.Val2321Leu) rs1085307523
NM_000384.3(APOB):c.7196A>G (p.Asp2399Gly)
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr)
NM_000384.3(APOB):c.7619G>T (p.Gly2540Val) rs571626569
NM_000384.3(APOB):c.7724_7729delinsTACGTC (p.Lys2575_Met2577delinsIleArgLeu) rs2103355216
NM_000384.3(APOB):c.7924C>T (p.Pro2642Ser) rs2103354999
NM_000384.3(APOB):c.7932G>C (p.Arg2644Ser) rs761712756
NM_000384.3(APOB):c.8045G>T (p.Ser2682Ile) rs375053331
NM_000384.3(APOB):c.8129A>G (p.Asp2710Gly) rs771882254
NM_000384.3(APOB):c.8381C>T (p.Thr2794Ile)
NM_000384.3(APOB):c.8531T>A (p.Leu2844Gln)
NM_000384.3(APOB):c.877A>G (p.Lys293Glu) rs2103381922
NM_000384.3(APOB):c.8882A>T (p.Asn2961Ile)
NM_000384.3(APOB):c.9175C>T (p.Arg3059Cys)
NM_000384.3(APOB):c.9242G>A (p.Ser3081Asn) rs72653100
NM_000384.3(APOB):c.9242G>C (p.Ser3081Thr) rs72653100

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.