ClinVar Miner

Variants in gene APOB with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 83
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HGVS dbSNP gnomAD frequency
NM_000384.3(APOB):c.293C>T (p.Thr98Ile) rs1367117 0.24155
NM_000384.3(APOB):c.10913G>A (p.Arg3638Gln) rs1801701 0.06584
NM_000384.3(APOB):c.433C>T (p.Pro145Ser) rs6752026 0.03579
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.2188G>A (p.Val730Ile) rs12691202 0.02673
NM_000384.3(APOB):c.3634C>A (p.Leu1212Met) rs61736761 0.02591
NM_000384.3(APOB):c.13441G>A (p.Ala4481Thr) rs1801695 0.02558
NM_000384.3(APOB):c.2222C>A (p.Thr741Asn) rs12714192 0.02253
NM_000384.3(APOB):c.8148C>T (p.Ile2716=) rs6413458 0.02201
NM_000384.3(APOB):c.10701G>A (p.Thr3567=) rs12713558 0.02176
NM_000384.3(APOB):c.9880T>C (p.Ser3294Pro) rs12720855 0.01525
NM_000384.3(APOB):c.9835A>G (p.Ser3279Gly) rs12720854 0.00761
NM_000384.3(APOB):c.3337G>C (p.Asp1113His) rs12713844 0.00735
NM_000384.3(APOB):c.1223T>C (p.Ile408Thr) rs12714225 0.00723
NM_000384.3(APOB):c.6895G>C (p.Asp2299His) rs12713681 0.00709
NM_000384.3(APOB):c.1594C>T (p.Arg532Trp) rs13306194 0.00578
NM_000384.3(APOB):c.12382G>A (p.Val4128Met) rs1801703 0.00562
NM_000384.3(APOB):c.10131G>A (p.Leu3377=) rs1799812 0.00560
NM_000384.3(APOB):c.12940A>G (p.Ile4314Val) rs72654423 0.00557
NM_000384.3(APOB):c.905-15C>G rs72653061 0.00554
NM_000384.3(APOB):c.3383G>A (p.Arg1128His) rs12713843 0.00376
NM_000384.3(APOB):c.8462C>T (p.Pro2821Leu) rs72653095 0.00267
NM_000384.3(APOB):c.10061C>G (p.Ala3354Gly) rs61742331 0.00256
NM_000384.3(APOB):c.10780T>C (p.Trp3594Arg) rs61744288 0.00256
NM_000384.3(APOB):c.7696G>A (p.Glu2566Lys) rs1801696 0.00249
NM_000384.3(APOB):c.11761G>A (p.Val3921Ile) rs72654409 0.00234
NM_000384.3(APOB):c.12766G>A (p.Glu4256Lys) rs61743313 0.00198
NM_000384.3(APOB):c.3427C>T (p.Pro1143Ser) rs72653077 0.00198
NM_000384.3(APOB):c.5066G>A (p.Arg1689His) rs151009667 0.00137
NM_000384.3(APOB):c.2068-4T>A rs41291161 0.00108
NM_000384.3(APOB):c.307T>C (p.Tyr103His) rs9282603 0.00108
NM_000384.3(APOB):c.7612C>T (p.Leu2538=) rs72653093 0.00102
NM_000384.3(APOB):c.3712C>A (p.Leu1238Ile) rs72653078 0.00091
NM_000384.3(APOB):c.4178C>T (p.Ala1393Val) rs143282164 0.00072
NM_000384.3(APOB):c.7285T>A (p.Ser2429Thr) rs72653092 0.00061
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu) rs41288783 0.00058
NM_000384.3(APOB):c.9322G>A (p.Glu3108Lys) rs140240214 0.00033
NM_000384.3(APOB):c.7619G>T (p.Gly2540Val) rs571626569 0.00029
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.10882A>T (p.Asn3628Tyr) rs141982176 0.00023
NM_000384.3(APOB):c.7181T>C (p.Val2394Ala) rs148429884 0.00023
NM_000384.3(APOB):c.925G>A (p.Ala309Thr) rs141888564 0.00022
NM_000384.3(APOB):c.3724T>A (p.Ser1242Thr) rs200261177 0.00019
NM_000384.3(APOB):c.3850C>T (p.Arg1284Trp) rs376768346 0.00015
NM_000384.3(APOB):c.6941T>C (p.Leu2314Pro) rs372035579 0.00015
NM_000384.3(APOB):c.7577T>C (p.Met2526Thr) rs373272476 0.00015
NM_000384.3(APOB):c.7006G>A (p.Ala2336Thr) rs146888928 0.00014
NM_000384.3(APOB):c.6969T>A (p.Asn2323Lys) rs138118085 0.00013
NM_000384.3(APOB):c.1010T>A (p.Ile337Asn) rs148126873 0.00012
NM_000384.3(APOB):c.5434G>T (p.Gly1812Trp) rs140174653 0.00012
NM_000384.3(APOB):c.1316G>A (p.Arg439Gln) rs61742990 0.00011
NM_000384.3(APOB):c.10700C>T (p.Thr3567Met) rs368278927 0.00009
NM_000384.3(APOB):c.11816G>A (p.Gly3939Asp) rs142828185 0.00009
NM_000384.3(APOB):c.9491C>T (p.Thr3164Met) rs143269114 0.00008
NM_000384.3(APOB):c.2312C>T (p.Pro771Leu) rs200524554 0.00007
NM_000384.3(APOB):c.9317A>G (p.Asn3106Ser) rs546747242 0.00006
NM_000384.3(APOB):c.3220G>A (p.Gly1074Arg) rs72653074 0.00005
NM_000384.3(APOB):c.13448C>T (p.Ala4483Val) rs147416761 0.00003
NM_000384.3(APOB):c.5991T>A (p.Asp1997Glu) rs768045701 0.00003
NM_000384.3(APOB):c.655C>T (p.Arg219Cys) rs145661815 0.00003
NM_000384.3(APOB):c.12025G>A (p.Val4009Met) rs140424976 0.00002
NM_000384.3(APOB):c.13463T>C (p.Ile4488Thr) rs374389311 0.00002
NM_000384.3(APOB):c.1595G>A (p.Arg532Gln) rs753831464 0.00002
NM_000384.3(APOB):c.3828C>A (p.Asn1276Lys) rs199966747 0.00002
NM_000384.3(APOB):c.4928C>T (p.Ala1643Val) rs1008238083 0.00002
NM_000384.3(APOB):c.6731G>A (p.Ser2244Asn) rs146333152 0.00002
NM_000384.3(APOB):c.7727G>A (p.Arg2576His) rs759057929 0.00002
NM_000384.3(APOB):c.11356C>T (p.Leu3786Phe) rs571485213 0.00001
NM_000384.3(APOB):c.12824A>C (p.Asp4275Ala) rs145807061 0.00001
NM_000384.3(APOB):c.13154G>A (p.Arg4385His) rs533755016 0.00001
NM_000384.3(APOB):c.2333G>A (p.Arg778His) rs201595604 0.00001
NM_000384.3(APOB):c.3829C>T (p.Leu1277Phe) rs544542990 0.00001
NM_000384.3(APOB):c.5580G>T (p.Gln1860His) rs199585500 0.00001
NM_000384.3(APOB):c.11477C>T (p.Thr3826Met) rs61744153
NM_000384.3(APOB):c.11744C>T (p.Ser3915Phe) rs201990496
NM_000384.3(APOB):c.1661C>T (p.Pro554Leu) rs12714214
NM_000384.3(APOB):c.2863C>T (p.Pro955Ser) rs13306206
NM_000384.3(APOB):c.4796G>A (p.Arg1599His) rs746414462
NM_000384.3(APOB):c.6636TGA[1] (p.Asp2213del) rs541497967
NM_000384.3(APOB):c.9242G>A (p.Ser3081Asn) rs72653100
NM_000384.3(APOB):c.9867C>A (p.Asp3289Glu) rs72654404

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