ClinVar Miner

Variants in gene OBSCN with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 129
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001386125.1(OBSCN):c.2894G>A (p.Arg965Lys) rs61560753 0.02514
NM_001386125.1(OBSCN):c.144G>A (p.Gln48=) rs114375717 0.01168
NM_001386125.1(OBSCN):c.8610C>G (p.Thr2870=) rs185248802 0.00977
NM_001386125.1(OBSCN):c.9803C>T (p.Ala3268Val) rs113447751 0.00929
NM_001386125.1(OBSCN):c.11521G>A (p.Gly3841Arg) rs56271332 0.00814
NM_001386125.1(OBSCN):c.16699C>T (p.Leu5567=) rs116642293 0.00811
NM_001386125.1(OBSCN):c.11984C>T (p.Pro3995Leu) rs62621834 0.00810
NM_001386125.1(OBSCN):c.21533-1980G>A rs114053815 0.00806
NM_001386125.1(OBSCN):c.19980T>A (p.Ser6660Arg) rs144372515 0.00796
NM_001386125.1(OBSCN):c.21533-2165C>T rs145544878 0.00776
NM_001386125.1(OBSCN):c.21533-1833G>A rs114510676 0.00756
NM_001386125.1(OBSCN):c.21533-2586C>T rs367920745 0.00728
NM_001386125.1(OBSCN):c.6447C>T (p.His2149=) rs138055037 0.00728
NM_001386125.1(OBSCN):c.16233G>A (p.Thr5411=) rs372827129 0.00726
NM_001386125.1(OBSCN):c.3141G>A (p.Ala1047=) rs140550965 0.00725
NM_001386125.1(OBSCN):c.2528G>A (p.Arg843His) rs141921462 0.00724
NM_001386125.1(OBSCN):c.10472T>G (p.Val3491Gly) rs202022683 0.00722
NM_001386125.1(OBSCN):c.7615C>G (p.Leu2539Val) rs201269256 0.00628
NM_001386125.1(OBSCN):c.4017T>C (p.Phe1339=) rs75365769 0.00605
NM_001386125.1(OBSCN):c.4020A>C (p.Gln1340His) rs199523598 0.00605
NM_001386125.1(OBSCN):c.15666G>A (p.Gln5222=) rs111731636 0.00602
NM_001386125.1(OBSCN):c.6403C>T (p.Arg2135Cys) rs114195142 0.00596
NM_001386125.1(OBSCN):c.18698G>A (p.Arg6233His) rs56015866 0.00583
NM_001386125.1(OBSCN):c.20169C>T (p.Asp6723=) rs142093978 0.00531
NM_001386125.1(OBSCN):c.11559G>A (p.Val3853=) rs111402242 0.00529
NM_001386125.1(OBSCN):c.8633T>C (p.Val2878Ala) rs200720682 0.00526
NM_001386125.1(OBSCN):c.2052C>T (p.Phe684=) rs112046759 0.00462
NM_001386125.1(OBSCN):c.5262C>T (p.Asp1754=) rs142188902 0.00434
NM_001386125.1(OBSCN):c.10722T>C (p.His3574=) rs75962730 0.00422
NM_001386125.1(OBSCN):c.1176C>T (p.Arg392=) rs185717159 0.00405
NM_001386125.1(OBSCN):c.20528A>G (p.Tyr6843Cys) rs200385051 0.00398
NM_001386125.1(OBSCN):c.25748C>T (p.Thr8583Met) rs184394044 0.00364
NM_001386125.1(OBSCN):c.18465C>T (p.Arg6155=) rs114969585 0.00356
NM_001386125.1(OBSCN):c.12634T>C (p.Ser4212Pro) rs147471011 0.00341
NM_001386125.1(OBSCN):c.8625C>T (p.Thr2875=) rs12030528 0.00336
NM_001386125.1(OBSCN):c.21533-1917G>A rs141233508 0.00326
NM_001386125.1(OBSCN):c.9424G>A (p.Ala3142Thr) rs191370080 0.00326
NM_001386125.1(OBSCN):c.11538G>T (p.Leu3846=) rs114473169 0.00324
NM_001386125.1(OBSCN):c.35T>A (p.Phe12Tyr) rs191837710 0.00322
NM_001386125.1(OBSCN):c.17179C>T (p.Arg5727Cys) rs186194072 0.00312
NM_001386125.1(OBSCN):c.11291C>T (p.Ala3764Val) rs55946300 0.00308
NM_001386125.1(OBSCN):c.16397G>A (p.Arg5466His) rs193004966 0.00307
NM_001386125.1(OBSCN):c.21533-2364G>A rs117551232 0.00302
NM_001386125.1(OBSCN):c.6407G>A (p.Arg2136His) rs28603121 0.00294
NM_001386125.1(OBSCN):c.4490G>A (p.Arg1497Gln) rs199874295 0.00291
NM_001386125.1(OBSCN):c.3162C>T (p.Cys1054=) rs12040506 0.00289
NM_001386125.1(OBSCN):c.16333C>G (p.His5445Asp) rs188287808 0.00261
NM_001386125.1(OBSCN):c.11031G>A (p.Pro3677=) rs79290523 0.00256
NM_001386125.1(OBSCN):c.9957C>T (p.Leu3319=) rs114058903 0.00212
NM_001386125.1(OBSCN):c.2342G>A (p.Arg781His) rs144514297 0.00208
NM_001386125.1(OBSCN):c.11457C>T (p.Pro3819=) rs56367754 0.00201
NM_001386125.1(OBSCN):c.9819G>A (p.Val3273=) rs112403932 0.00184
NM_001386125.1(OBSCN):c.21214C>G (p.Arg7072Gly) rs142615706 0.00172
NM_001386125.1(OBSCN):c.2328C>T (p.Tyr776=) rs369447003 0.00172
NM_001386125.1(OBSCN):c.9842G>A (p.Arg3281Gln) rs188024384 0.00162
NM_001386125.1(OBSCN):c.8343C>T (p.His2781=) rs376684253 0.00150
NM_001386125.1(OBSCN):c.23303C>A (p.Pro7768His) rs201092597 0.00149
NM_001386125.1(OBSCN):c.15509G>A (p.Arg5170His) rs56306215 0.00140
NM_001386125.1(OBSCN):c.11061C>T (p.Phe3687=) rs369584483 0.00134
NM_001386125.1(OBSCN):c.20115C>T (p.Gly6705=) rs140147625 0.00124
NM_001386125.1(OBSCN):c.7302C>T (p.Cys2434=) rs369558704 0.00124
NM_001386125.1(OBSCN):c.3288C>T (p.Cys1096=) rs373806868 0.00120
NM_001386125.1(OBSCN):c.4393G>A (p.Glu1465Lys) rs201854668 0.00116
NM_001386125.1(OBSCN):c.11853C>T (p.Cys3951=) rs200826459 0.00114
NM_001386125.1(OBSCN):c.16361A>T (p.Gln5454Leu) rs116329268 0.00108
NM_001386125.1(OBSCN):c.24417C>T (p.Arg8139=) rs499309 0.00105
NM_001386125.1(OBSCN):c.16425C>T (p.Thr5475=) rs373494343 0.00102
NM_001386125.1(OBSCN):c.18062C>T (p.Ala6021Val) rs56359770 0.00093
NM_001386125.1(OBSCN):c.21303C>T (p.Asp7101=) rs56187628 0.00092
NM_001386125.1(OBSCN):c.18705C>A (p.Ala6235=) rs56025664 0.00089
NM_001386125.1(OBSCN):c.17174C>T (p.Ser5725Leu) rs181568906 0.00083
NM_001386125.1(OBSCN):c.16015A>G (p.Thr5339Ala) rs183406337 0.00078
NM_001386125.1(OBSCN):c.20502G>A (p.Lys6834=) rs191140144 0.00078
NM_001386125.1(OBSCN):c.16853A>C (p.Glu5618Ala) rs200399314 0.00076
NM_001386125.1(OBSCN):c.9672G>A (p.Val3224=) rs3795784 0.00074
NM_001386125.1(OBSCN):c.9065A>G (p.Asn3022Ser) rs113202278 0.00072
NM_001386125.1(OBSCN):c.1899C>T (p.Ser633=) rs193175485 0.00069
NM_001386125.1(OBSCN):c.16251C>T (p.Pro5417=) rs117435683 0.00056
NM_001386125.1(OBSCN):c.9040G>C (p.Asp3014His) rs202052558 0.00056
NM_001386125.1(OBSCN):c.24984A>G (p.Ser8328=) rs370699889 0.00046
NM_001386125.1(OBSCN):c.20378T>C (p.Val6793Ala) rs200917956 0.00038
NM_001386125.1(OBSCN):c.15217G>A (p.Glu5073Lys) rs201877667 0.00032
NM_001386125.1(OBSCN):c.19850C>T (p.Ala6617Val) rs191098985 0.00032
NM_001386125.1(OBSCN):c.23350C>T (p.Arg7784Trp) rs369885852 0.00031
NM_001386125.1(OBSCN):c.10115C>T (p.Ala3372Val) rs199933567 0.00026
NM_001386125.1(OBSCN):c.12420C>T (p.Ala4140=) rs199641194 0.00024
NM_001386125.1(OBSCN):c.20021G>A (p.Ser6674Asn) rs376194851 0.00019
NM_001386125.1(OBSCN):c.3099A>G (p.Thr1033=) rs202097101 0.00019
NM_001386125.1(OBSCN):c.12345C>T (p.Leu4115=) rs527943941 0.00018
NM_001386125.1(OBSCN):c.16503A>G (p.Ala5501=) rs370547153 0.00016
NM_001386125.1(OBSCN):c.15633G>A (p.Glu5211=) rs529583811 0.00006
NM_001386125.1(OBSCN):c.4797G>A (p.Ala1599=) rs372472787 0.00004
NM_001386125.1(OBSCN):c.18006C>T (p.Pro6002=) rs534386095 0.00002
NM_001386125.1(OBSCN):c.8631C>T (p.Pro2877=) rs781325246 0.00001
NM_001386125.1(OBSCN):c.12234G>A (p.Leu4078=)
NM_001386125.1(OBSCN):c.15282C>T (p.Gly5094=)
NM_001386125.1(OBSCN):c.16339G>A (p.Ala5447Thr)
NM_001386125.1(OBSCN):c.1692C>T (p.His564=)
NM_001386125.1(OBSCN):c.17438G>A (p.Arg5813His)
NM_001386125.1(OBSCN):c.17759G>A (p.Arg5920His)
NM_001386125.1(OBSCN):c.18010G>T (p.Asp6004Tyr)
NM_001386125.1(OBSCN):c.18456C>T (p.Gly6152=)
NM_001386125.1(OBSCN):c.19271C>T (p.Ser6424Leu)
NM_001386125.1(OBSCN):c.19394G>T (p.Gly6465Val)
NM_001386125.1(OBSCN):c.20055C>A (p.His6685Gln)
NM_001386125.1(OBSCN):c.21282G>T (p.Pro7094=) rs372931114
NM_001386125.1(OBSCN):c.21532+3123C>T
NM_001386125.1(OBSCN):c.21533-2163C>T
NM_001386125.1(OBSCN):c.21533-2450G>C
NM_001386125.1(OBSCN):c.21533-2508C>T
NM_001386125.1(OBSCN):c.21533-2727G>A
NM_001386125.1(OBSCN):c.21533-2783C>G
NM_001386125.1(OBSCN):c.22155C>G (p.Thr7385=)
NM_001386125.1(OBSCN):c.2279G>A (p.Arg760Gln)
NM_001386125.1(OBSCN):c.23056G>A (p.Glu7686Lys)
NM_001386125.1(OBSCN):c.23281G>C (p.Ala7761Pro)
NM_001386125.1(OBSCN):c.23344T>G (p.Phe7782Val)
NM_001386125.1(OBSCN):c.23385_23386del (p.Ala7795_Ser7796insTer)
NM_001386125.1(OBSCN):c.23838del (p.Ser7947fs)
NM_001386125.1(OBSCN):c.24709G>A (p.Val8237Met)
NM_001386125.1(OBSCN):c.25852C>T (p.Arg8618Trp)
NM_001386125.1(OBSCN):c.25956G>A (p.Gly8652=)
NM_001386125.1(OBSCN):c.496G>A (p.Ala166Thr)
NM_001386125.1(OBSCN):c.509G>C (p.Arg170Pro)
NM_001386125.1(OBSCN):c.6253C>T (p.His2085Tyr)
NM_001386125.1(OBSCN):c.8103T>G (p.Phe2701Leu)
NM_001386125.1(OBSCN):c.8913G>A (p.Ala2971=)
NM_001386125.1(OBSCN):c.8997G>A (p.Thr2999=)
NM_001386125.1(OBSCN):c.9336C>T (p.Gly3112=)

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.