ClinVar Miner

List of variants reported as likely benign for gingival disorder

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 156
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HGVS dbSNP gnomAD frequency
NM_005633.4(SOS1):c.345+15C>T rs75937422 0.00407
NM_005633.4(SOS1):c.2997T>C (p.Asn999=) rs145364368 0.00352
NM_005633.4(SOS1):c.2673+14T>C rs183998234 0.00304
NM_005633.4(SOS1):c.2122G>A (p.Ala708Thr) rs140811086 0.00280
NM_005633.4(SOS1):c.570C>T (p.Asp190=) rs55980502 0.00233
NM_002029.4(FPR1):c.607A>G (p.Ile203Val) rs150239733 0.00230
NM_005633.4(SOS1):c.3081+13A>G rs189695571 0.00223
NM_002029.4(FPR1):c.26C>T (p.Thr9Met) rs148095693 0.00215
NM_005633.4(SOS1):c.3032A>G (p.Asn1011Ser) rs8192671 0.00164
NM_005633.4(SOS1):c.2238T>C (p.Asn746=) rs75877625 0.00084
NM_005633.4(SOS1):c.73C>T (p.Pro25Ser) rs139592595 0.00082
NM_002029.4(FPR1):c.368G>A (p.Arg123His) rs149931707 0.00041
NM_005612.5(REST):c.898+15C>T rs148949163 0.00026
NM_005633.4(SOS1):c.1705C>G (p.Leu569Val) rs200786705 0.00019
NM_005633.4(SOS1):c.1489C>A (p.Arg497=) rs542368621 0.00018
NM_002029.4(FPR1):c.858A>G (p.Thr286=) rs371692364 0.00017
NM_002029.4(FPR1):c.553A>G (p.Asn185Asp) rs145973159 0.00016
NM_002029.4(FPR1):c.84C>T (p.Ile28=) rs143690932 0.00016
NM_005633.4(SOS1):c.2966G>A (p.Arg989Lys) rs202043599 0.00016
NM_002029.4(FPR1):c.1044G>A (p.Gln348=) rs150820622 0.00014
NM_005633.4(SOS1):c.1962G>A (p.Glu654=) rs144382701 0.00014
NM_002029.4(FPR1):c.744A>C (p.Ala248=) rs145578657 0.00013
NM_005633.4(SOS1):c.1668A>C (p.Val556=) rs376314461 0.00013
NM_002029.4(FPR1):c.132C>T (p.Asn44=) rs762415254 0.00011
NM_005633.4(SOS1):c.3357C>T (p.Thr1119=) rs373319212 0.00011
NM_002029.4(FPR1):c.414C>T (p.Thr138=) rs151277630 0.00010
NM_005633.4(SOS1):c.1269C>T (p.Asn423=) rs138459502 0.00010
NM_005633.4(SOS1):c.1566T>C (p.Asn522=) rs145325119 0.00010
NM_002029.4(FPR1):c.639C>T (p.Pro213=) rs141229910 0.00009
NM_005633.4(SOS1):c.2510+19C>G rs375675348 0.00009
NM_002029.4(FPR1):c.957T>C (p.Ser319=) rs375541232 0.00008
NM_002029.4(FPR1):c.378C>T (p.Cys126=) rs776424230 0.00007
NM_002029.4(FPR1):c.582C>T (p.Ala194=) rs747540806 0.00007
NM_005633.4(SOS1):c.1854C>T (p.Tyr618=) rs727505181 0.00007
NM_005633.4(SOS1):c.3269C>T (p.Pro1090Leu) rs730881034 0.00007
NM_002029.4(FPR1):c.330C>T (p.Phe110=) rs539229723 0.00006
NM_002029.4(FPR1):c.564A>G (p.Lys188=) rs369805689 0.00006
NM_005633.4(SOS1):c.929G>A (p.Arg310His) rs143481916 0.00006
NM_002029.4(FPR1):c.519A>T (p.Thr173=) rs748615602 0.00005
NM_005633.4(SOS1):c.587C>T (p.Ser196Leu) rs199898869 0.00005
NM_002029.4(FPR1):c.189T>C (p.Ser63=) rs148014099 0.00004
NM_002029.4(FPR1):c.381C>T (p.Val127=) rs760563008 0.00004
NM_002029.4(FPR1):c.555C>T (p.Asn185=) rs539893573 0.00004
NM_005633.4(SOS1):c.1095A>G (p.Glu365=) rs767540464 0.00004
NM_005633.4(SOS1):c.1490G>A (p.Arg497Gln) rs371314838 0.00004
NM_005633.4(SOS1):c.1621T>C (p.Leu541=) rs371286473 0.00004
NM_005633.4(SOS1):c.1842G>A (p.Thr614=) rs143750479 0.00004
NM_005633.4(SOS1):c.1905C>T (p.Cys635=) rs762900789 0.00004
NM_005633.4(SOS1):c.3942C>T (p.His1314=) rs778838515 0.00004
NM_002029.4(FPR1):c.738C>T (p.Val246=) rs148898220 0.00003
NM_002029.4(FPR1):c.942C>T (p.His314=) rs749154560 0.00003
NM_005633.4(SOS1):c.66A>G (p.Leu22=) rs770539511 0.00003
NM_005633.4(SOS1):c.9G>A (p.Ala3=) rs566601513 0.00003
NM_002029.4(FPR1):c.472T>C (p.Leu158=) rs1471159412 0.00002
NM_002029.4(FPR1):c.513G>A (p.Thr171=) rs554681504 0.00002
NM_002029.4(FPR1):c.543G>A (p.Ser181=) rs753325158 0.00002
NM_002029.4(FPR1):c.954C>G (p.Ala318=) rs766700447 0.00002
NM_005633.4(SOS1):c.1251A>C (p.Leu417=) rs144027132 0.00002
NM_005633.4(SOS1):c.2007C>G (p.Pro669=) rs529749913 0.00002
NM_005633.4(SOS1):c.3347-3C>T rs779326746 0.00002
NM_005633.4(SOS1):c.3384T>C (p.His1128=) rs1412775460 0.00002
NM_005633.4(SOS1):c.396A>T (p.Ala132=) rs727505385 0.00002
NM_005633.4(SOS1):c.87+12G>T rs368569135 0.00002
NM_002029.4(FPR1):c.156A>T (p.Gly52=) rs1389132373 0.00001
NM_002029.4(FPR1):c.21C>G (p.Leu7=) rs895586771 0.00001
NM_002029.4(FPR1):c.27G>A (p.Thr9=) rs771642804 0.00001
NM_002029.4(FPR1):c.300C>T (p.Phe100=) rs199764870 0.00001
NM_002029.4(FPR1):c.339C>A (p.Val113=) rs778269740 0.00001
NM_002029.4(FPR1):c.42G>A (p.Gly14=) rs866728748 0.00001
NM_002029.4(FPR1):c.474G>A (p.Leu158=) rs753449716 0.00001
NM_002029.4(FPR1):c.528C>T (p.Cys176=) rs769223294 0.00001
NM_005633.4(SOS1):c.1191A>G (p.Lys397=) rs770175415 0.00001
NM_005633.4(SOS1):c.1458A>G (p.Ala486=) rs772746896 0.00001
NM_005633.4(SOS1):c.1848T>C (p.His616=) rs1344852617 0.00001
NM_005633.4(SOS1):c.1863C>T (p.Pro621=) rs759125551 0.00001
NM_005633.4(SOS1):c.1956G>A (p.Glu652=) rs1365773428 0.00001
NM_005633.4(SOS1):c.1995T>C (p.Asn665=) rs779262456 0.00001
NM_005633.4(SOS1):c.2454T>C (p.Ser818=) rs748802612 0.00001
NM_005633.4(SOS1):c.2604T>C (p.Phe868=) rs756520305 0.00001
NM_005633.4(SOS1):c.2739G>A (p.Lys913=) rs997339872 0.00001
NM_005633.4(SOS1):c.3033C>T (p.Asn1011=) rs1196614292 0.00001
NM_005633.4(SOS1):c.3060C>T (p.Asn1020=) rs142431345 0.00001
NM_005633.4(SOS1):c.3093T>C (p.Tyr1031=) rs766864647 0.00001
NM_005633.4(SOS1):c.3114T>G (p.Pro1038=) rs777755307 0.00001
NM_005633.4(SOS1):c.3282T>G (p.Gly1094=) rs145357714 0.00001
NM_005633.4(SOS1):c.3438A>G (p.Glu1146=) rs1226908698 0.00001
NM_005633.4(SOS1):c.3504A>G (p.Pro1168=) rs748617507 0.00001
NM_005633.4(SOS1):c.3732T>C (p.His1244=) rs1391583247 0.00001
NM_005633.4(SOS1):c.3795T>G (p.Ser1265=) rs538954728 0.00001
NM_005633.4(SOS1):c.3832T>C (p.Leu1278=) rs750354913 0.00001
NM_005633.4(SOS1):c.3987T>C (p.Asn1329=) rs936986823 0.00001
NM_005633.4(SOS1):c.429G>A (p.Lys143=) rs773264070 0.00001
NM_005633.4(SOS1):c.543A>G (p.Glu181=) rs201068374 0.00001
NM_005633.4(SOS1):c.552T>C (p.Asn184=) rs727503438 0.00001
NM_005633.4(SOS1):c.783C>A (p.Gly261=) rs951992465 0.00001
NM_005633.4(SOS1):c.795T>C (p.Asp265=) rs777745085 0.00001
NM_005633.4(SOS1):c.984C>T (p.Gly328=) rs778223456 0.00001
NM_002029.4(FPR1):c.1008C>A (p.Thr336=)
NM_002029.4(FPR1):c.1008C>T (p.Thr336=)
NM_002029.4(FPR1):c.12T>C (p.Asn4=) rs1479199724
NM_002029.4(FPR1):c.144C>T (p.Ile48=)
NM_002029.4(FPR1):c.15C>T (p.Ser5=)
NM_002029.4(FPR1):c.17C>T (p.Ser6Phe)
NM_002029.4(FPR1):c.204C>T (p.Ala68=) rs143480239
NM_002029.4(FPR1):c.258C>T (p.Ala86=)
NM_002029.4(FPR1):c.279C>T (p.Phe93=)
NM_002029.4(FPR1):c.27G>C (p.Thr9=) rs771642804
NM_002029.4(FPR1):c.30C>T (p.Asn10=) rs371185306
NM_002029.4(FPR1):c.333A>G (p.Gly111=)
NM_002029.4(FPR1):c.390A>G (p.Pro130=) rs2122323286
NM_002029.4(FPR1):c.405C>T (p.Asn135=)
NM_002029.4(FPR1):c.408C>T (p.His136=)
NM_002029.4(FPR1):c.439A>T (p.Ile147Phe) rs183314714
NM_002029.4(FPR1):c.444G>T (p.Gly148=)
NM_002029.4(FPR1):c.447C>T (p.Pro149=) rs778341723
NM_002029.4(FPR1):c.453G>A (p.Val151=) rs2122322988
NM_002029.4(FPR1):c.465C>T (p.Leu155=)
NM_002029.4(FPR1):c.486T>C (p.Ile162=) rs1848258347
NM_002029.4(FPR1):c.618C>T (p.Phe206=) rs2122322070
NM_002029.4(FPR1):c.624T>C (p.Ile208=)
NM_002029.4(FPR1):c.648C>T (p.Ile216=)
NM_002029.4(FPR1):c.696C>G (p.Gly232=)
NM_002029.4(FPR1):c.69C>T (p.Leu23=)
NM_002029.4(FPR1):c.705G>A (p.Lys235=) rs1599806461
NM_002029.4(FPR1):c.723G>T (p.Arg241=)
NM_002029.4(FPR1):c.726C>A (p.Val242=)
NM_002029.4(FPR1):c.726C>T (p.Val242=) rs143583727
NM_002029.4(FPR1):c.876C>T (p.Phe292=)
NM_002029.4(FPR1):c.918G>A (p.Gln306=)
NM_002029.4(FPR1):c.934C>T (p.Leu312=) rs2083741372
NM_002029.4(FPR1):c.960G>A (p.Leu320=)
NM_002029.4(FPR1):c.969C>T (p.Ala323=) rs2122320667
NM_002029.4(FPR1):c.975C>G (p.Thr325=) rs768152901
NM_005612.5(REST):c.3098A>G (p.His1033Arg) rs572949989
NM_005633.4(SOS1):c.*1606del rs34248802
NM_005633.4(SOS1):c.*2244_*2245dup rs3832123
NM_005633.4(SOS1):c.1035C>G (p.Ala345=) rs557313301
NM_005633.4(SOS1):c.1203-8T>C rs1669853901
NM_005633.4(SOS1):c.1707G>A (p.Leu569=) rs1479407572
NM_005633.4(SOS1):c.2063+44T>C rs111576630
NM_005633.4(SOS1):c.2064-20A>T rs756707478
NM_005633.4(SOS1):c.213+14_213+16del rs768872084
NM_005633.4(SOS1):c.21C>T (p.Pro7=) rs727504845
NM_005633.4(SOS1):c.2517T>C (p.Ile839=) rs776366413
NM_005633.4(SOS1):c.2674-9del rs532594344
NM_005633.4(SOS1):c.2674-9dup rs532594344
NM_005633.4(SOS1):c.273A>G (p.Gln91=) rs914110575
NM_005633.4(SOS1):c.2775A>T (p.Pro925=) rs397517160
NM_005633.4(SOS1):c.3195T>C (p.Tyr1065=) rs1280224224
NM_005633.4(SOS1):c.3693A>G (p.Leu1231=) rs772625418
NM_005633.4(SOS1):c.3813G>A (p.Arg1271=) rs863224405
NM_005633.4(SOS1):c.511-9_511-6del rs986512473
NM_005633.4(SOS1):c.706T>C (p.Leu236=) rs1418372765
NM_005633.4(SOS1):c.771A>G (p.Val257=) rs1671007109
NM_005633.4(SOS1):c.891G>A (p.Ser297=) rs1572841459
NM_005633.4(SOS1):c.976-5dup rs771586560

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