ClinVar Miner

List of variants in gene ITGB4 reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 118
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000213.5(ITGB4):c.1821G>A (p.Ser607=) rs2290460 0.05352
NM_000213.5(ITGB4):c.702C>T (p.Gly234=) rs61751843 0.02922
NM_000213.5(ITGB4):c.3729G>A (p.Pro1243=) rs61735289 0.02599
NM_000213.5(ITGB4):c.513T>C (p.Phe171=) rs148048907 0.01650
NM_000213.5(ITGB4):c.1544G>A (p.Arg515His) rs61735297 0.01220
NM_000213.5(ITGB4):c.1377+15C>T rs78048168 0.01106
NM_000213.5(ITGB4):c.1667G>A (p.Arg556His) rs142562582 0.00745
NM_000213.5(ITGB4):c.1893C>G (p.Ser631=) rs61735295 0.00640
NM_000213.5(ITGB4):c.-125G>C rs552008042 0.00591
NM_000213.5(ITGB4):c.2730C>T (p.Ala910=) rs61735292 0.00454
NM_000213.5(ITGB4):c.867C>T (p.His289=) rs150113215 0.00384
NM_000213.5(ITGB4):c.2207G>T (p.Cys736Phe) rs143203816 0.00370
NM_000213.5(ITGB4):c.2115C>A (p.Asp705Glu) rs62639300 0.00357
NM_000213.5(ITGB4):c.2701C>T (p.Leu901Phe) rs145644205 0.00272
NM_000213.5(ITGB4):c.1434G>T (p.Gln478His) rs8079267 0.00227
NM_000213.5(ITGB4):c.-68C>T rs571564589 0.00215
NM_000213.5(ITGB4):c.2929C>T (p.Arg977Cys) rs145976111 0.00214
NM_000213.5(ITGB4):c.1533G>A (p.Pro511=) rs148312483 0.00145
NM_000213.5(ITGB4):c.282C>T (p.Thr94=) rs146609350 0.00143
NM_000213.5(ITGB4):c.3112-3C>T rs151033645 0.00138
NM_000213.5(ITGB4):c.3598G>A (p.Gly1200Arg) rs75129664 0.00136
NM_000213.5(ITGB4):c.1345G>A (p.Gly449Ser) rs147963396 0.00135
NM_000213.5(ITGB4):c.2922C>T (p.Leu974=) rs139130590 0.00093
NM_000213.5(ITGB4):c.2638G>A (p.Asp880Asn) rs139092703 0.00086
NM_000213.5(ITGB4):c.1428C>T (p.Cys476=) rs149030156 0.00081
NM_000213.5(ITGB4):c.3501C>T (p.Ser1167=) rs141513851 0.00070
NM_000213.5(ITGB4):c.1924G>A (p.Glu642Lys) rs200371855 0.00068
NM_000213.5(ITGB4):c.2918C>A (p.Thr973Asn) rs146391318 0.00065
NM_000213.5(ITGB4):c.1884C>T (p.Asp628=) rs140078827 0.00059
NM_000213.5(ITGB4):c.1181G>A (p.Arg394Lys) rs144655991 0.00048
NM_000213.5(ITGB4):c.1002+12A>G rs374003966 0.00044
NM_000213.5(ITGB4):c.1032A>G (p.Ser344=) rs145591069 0.00043
NM_000213.5(ITGB4):c.1749C>T (p.Ile583=) rs144302042 0.00041
NM_000213.5(ITGB4):c.2145C>T (p.Ile715=) rs140999738 0.00041
NM_000213.5(ITGB4):c.1095G>A (p.Arg365=) rs141970956 0.00039
NM_000213.5(ITGB4):c.1666C>T (p.Arg556Cys) rs150166497 0.00038
NM_000213.5(ITGB4):c.2108A>G (p.Lys703Arg) rs56119997 0.00035
NM_000213.5(ITGB4):c.2123C>T (p.Pro708Leu) rs146500584 0.00035
NM_000213.5(ITGB4):c.-23T>C rs886053407 0.00034
NM_000213.5(ITGB4):c.162+9C>T rs200853535 0.00029
NM_000213.5(ITGB4):c.2503C>G (p.Pro835Ala) rs183705877 0.00029
NM_000213.5(ITGB4):c.3057C>T (p.Gly1019=) rs139146525 0.00029
NM_000213.5(ITGB4):c.1056G>A (p.Ser352=) rs187527294 0.00028
NM_000213.5(ITGB4):c.1377+7C>T rs200004156 0.00022
NM_000213.5(ITGB4):c.2674C>T (p.Arg892Cys) rs139933962 0.00022
NM_000213.5(ITGB4):c.495C>T (p.Ser165=) rs75092172 0.00020
NM_000213.5(ITGB4):c.708C>T (p.Phe236=) rs146923910 0.00019
NM_000213.5(ITGB4):c.738+3G>A rs374647847 0.00018
NM_000213.5(ITGB4):c.2634-8C>T rs749527800 0.00016
NM_000213.5(ITGB4):c.2833C>T (p.Arg945Trp) rs150668075 0.00016
NM_000213.5(ITGB4):c.759G>A (p.Pro253=) rs776214034 0.00016
NM_000213.5(ITGB4):c.1262C>T (p.Thr421Met) rs148535298 0.00014
NM_000213.5(ITGB4):c.210G>A (p.Ala70=) rs200500313 0.00014
NM_000213.5(ITGB4):c.2670G>A (p.Ala890=) rs146449374 0.00012
NM_000213.5(ITGB4):c.3624C>T (p.Ser1208=) rs145928221 0.00012
NM_000213.5(ITGB4):c.1201C>T (p.Arg401Trp) rs200122430 0.00011
NM_000213.5(ITGB4):c.2784C>T (p.Asp928=) rs201900480 0.00011
NM_000213.5(ITGB4):c.1593C>T (p.Tyr531=) rs778102219 0.00010
NM_000213.5(ITGB4):c.312A>G (p.Gln104=) rs568835164 0.00009
NM_000213.5(ITGB4):c.1805A>T (p.His602Leu) rs201103623 0.00007
NM_000213.5(ITGB4):c.2578G>A (p.Gly860Ser) rs201523797 0.00007
NM_000213.5(ITGB4):c.3205T>C (p.Ser1069Pro) rs530916890 0.00007
NM_000213.5(ITGB4):c.1136G>A (p.Arg379Gln) rs367872059 0.00006
NM_000213.5(ITGB4):c.1936C>T (p.Arg646Cys) rs201350965 0.00006
NM_000213.5(ITGB4):c.2025C>T (p.Asp675=) rs202097958 0.00006
NM_000213.5(ITGB4):c.2834G>A (p.Arg945Gln) rs141953294 0.00006
NM_000213.5(ITGB4):c.1179G>A (p.Thr393=) rs772335175 0.00005
NM_000213.5(ITGB4):c.1413C>T (p.Asn471=) rs375790655 0.00005
NM_000213.5(ITGB4):c.2830G>A (p.Val944Ile) rs770396319 0.00005
NM_000213.5(ITGB4):c.859C>T (p.Arg287Trp) rs140750952 0.00005
NM_000213.5(ITGB4):c.2241G>A (p.Pro747=) rs377428995 0.00004
NM_000213.5(ITGB4):c.2962+14G>A rs369351466 0.00004
NM_000213.5(ITGB4):c.3215G>A (p.Arg1072Gln) rs750423295 0.00004
NM_000213.5(ITGB4):c.852C>T (p.Asn284=) rs529755730 0.00004
NM_000213.5(ITGB4):c.1093C>T (p.Arg365Trp) rs886053408 0.00003
NM_000213.5(ITGB4):c.1581C>T (p.Gly527=) rs374868983 0.00003
NM_000213.5(ITGB4):c.3655+10C>T rs767096926 0.00003
NM_000213.5(ITGB4):c.1113C>T (p.Asp371=) rs772224695 0.00002
NM_000213.5(ITGB4):c.2782+10C>T rs757546708 0.00002
NM_000213.5(ITGB4):c.3317A>G (p.Asp1106Gly) rs370112615 0.00002
NM_000213.5(ITGB4):c.3463A>G (p.Met1155Val) rs756806922 0.00002
NM_000213.5(ITGB4):c.595C>A (p.Pro199Thr) rs780182739 0.00002
NM_000213.5(ITGB4):c.1539C>T (p.Ser513=) rs886053410 0.00001
NM_000213.5(ITGB4):c.1560C>T (p.Cys520=) rs538635871 0.00001
NM_000213.5(ITGB4):c.1972G>T (p.Val658Leu) rs747235341 0.00001
NM_000213.5(ITGB4):c.2067C>T (p.Asp689=) rs1020515752 0.00001
NM_000213.5(ITGB4):c.2371C>T (p.Arg791Cys) rs1368715042 0.00001
NM_000213.5(ITGB4):c.2551-10T>C rs1294215890 0.00001
NM_000213.5(ITGB4):c.2609+7C>T rs368466242 0.00001
NM_000213.5(ITGB4):c.2625C>T (p.Ala875=) rs561694657 0.00001
NM_000213.5(ITGB4):c.2755G>A (p.Gly919Ser) rs372890193 0.00001
NM_000213.5(ITGB4):c.2865C>T (p.Asp955=) rs780448706 0.00001
NM_000213.5(ITGB4):c.2962+11G>A rs554755694 0.00001
NM_000213.5(ITGB4):c.299A>G (p.Gln100Arg) rs750443550 0.00001
NM_000213.5(ITGB4):c.3097G>A (p.Ala1033Thr) rs763215637 0.00001
NM_000213.5(ITGB4):c.3338C>T (p.Thr1113Met) rs775373022 0.00001
NM_000213.5(ITGB4):c.-159A>C rs1473747702
NM_000213.5(ITGB4):c.1210G>A (p.Glu404Lys) rs886053409
NM_000213.5(ITGB4):c.1461C>T (p.Gly487=) rs2060908227
NM_000213.5(ITGB4):c.1860+10A>C rs8065184
NM_000213.5(ITGB4):c.1945G>A (p.Glu649Lys) rs886053411
NM_000213.5(ITGB4):c.1968G>T (p.Lys656Asn) rs377703595
NM_000213.5(ITGB4):c.2009G>A (p.Arg670His) rs149659118
NM_000213.5(ITGB4):c.2422G>A (p.Ala808Thr) rs147480547
NM_000213.5(ITGB4):c.2503C>A (p.Pro835Thr) rs183705877
NM_000213.5(ITGB4):c.2550+1G>A rs545619665
NM_000213.5(ITGB4):c.2886G>A (p.Val962=) rs886053412
NM_000213.5(ITGB4):c.2962+5G>T rs918899742
NM_000213.5(ITGB4):c.3099G>A (p.Ala1033=) rs145314226
NM_000213.5(ITGB4):c.3230G>T (p.Arg1077Leu) rs201487753
NM_000213.5(ITGB4):c.3232C>G (p.Arg1078Gly) rs564989714
NM_000213.5(ITGB4):c.3384C>T (p.Gly1128=) rs111568842
NM_000213.5(ITGB4):c.3430C>G (p.His1144Asp) rs765807271
NM_000213.5(ITGB4):c.346C>T (p.Arg116Trp) rs146269824
NM_000213.5(ITGB4):c.3765C>G (p.Val1255=) rs2061357111
NM_000213.5(ITGB4):c.690T>A (p.Asp230Glu) rs2060802259
NM_000213.5(ITGB4):c.754C>A (p.Arg252Ser) rs201494421
NM_000213.5(ITGB4):c.93G>C (p.Lys31Asn) rs2060737043

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.