ClinVar Miner

List of variants in gene ACVR2B reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_001106.4(ACVR2B):c.*3090C>T rs11926767 0.60530
NM_001106.4(ACVR2B):c.*4617C>G rs6599205 0.60080
NM_001106.4(ACVR2B):c.*911C>T rs6599204 0.60049
NM_001106.4(ACVR2B):c.333A>G (p.Glu111=) rs2070489 0.51926
NM_001106.4(ACVR2B):c.*8512A>C rs13072731 0.48169
NM_001106.4(ACVR2B):c.*2392T>C rs11914389 0.44215
NM_001106.4(ACVR2B):c.811-13T>C rs13097628 0.42596
NM_001106.4(ACVR2B):c.*7688G>A rs1058945 0.42327
NM_001106.4(ACVR2B):c.*744T>C rs7642472 0.42268
NM_001106.4(ACVR2B):c.1458C>T (p.Asn486=) rs1046048 0.42251
NM_001106.4(ACVR2B):c.*4995C>T rs7433277 0.42110
NM_001106.4(ACVR2B):c.*5002C>T rs2370840 0.38903
NM_001106.4(ACVR2B):c.*9319T>A rs77317995 0.22367
NM_001106.4(ACVR2B):c.*9471C>T rs6802919 0.09331
NM_001106.4(ACVR2B):c.*5256A>G rs62239941 0.05920
NM_001106.4(ACVR2B):c.*2280A>G rs17037775 0.05902
NM_001106.4(ACVR2B):c.*765G>A rs12636077 0.05884
NM_001106.4(ACVR2B):c.*6948G>A rs62241768 0.05874
NM_001106.4(ACVR2B):c.*501G>C rs61085191 0.05701
NM_001106.4(ACVR2B):c.*2900T>C rs62239939 0.05513
NM_001106.4(ACVR2B):c.*2425G>A rs76799785 0.03558
NM_001106.4(ACVR2B):c.*3316G>A rs6790964 0.02867
NM_001106.4(ACVR2B):c.*8141C>A rs114378912 0.01477
NM_001106.4(ACVR2B):c.*3748G>T rs2169551 0.01409
NM_001106.4(ACVR2B):c.1344+7G>T rs9876823 0.01406
NM_001106.4(ACVR2B):c.*7379G>A rs115907825 0.01331
NM_001106.4(ACVR2B):c.*87A>G rs78099173 0.01074
NM_001106.4(ACVR2B):c.*6173A>C rs76892072 0.00862
NM_001106.4(ACVR2B):c.*1957T>G rs115223892 0.00774
NM_001106.4(ACVR2B):c.*3127G>A rs139847458 0.00714
NM_001106.4(ACVR2B):c.*3956A>G rs77091454 0.00709
NM_001106.4(ACVR2B):c.1075-5C>T rs115155428 0.00657
NM_001106.4(ACVR2B):c.*8187G>A rs116523268 0.00605
NM_001106.4(ACVR2B):c.*476C>T rs79453833 0.00560
NM_001106.4(ACVR2B):c.*338C>G rs78458694 0.00515
NM_001106.4(ACVR2B):c.*6553G>A rs75944257 0.00499
NM_001106.4(ACVR2B):c.*4963T>A rs59630626 0.00437
NM_001106.4(ACVR2B):c.*1042G>A rs541363749 0.00379
NM_001106.4(ACVR2B):c.*2042C>T rs187282638 0.00378
NM_001106.4(ACVR2B):c.*592C>T rs80046041 0.00349
NM_001106.4(ACVR2B):c.*1375C>T rs193122447 0.00318
NM_001106.4(ACVR2B):c.811-12G>A rs144849143 0.00302
NM_001106.4(ACVR2B):c.*204C>T rs183119680 0.00301
NM_001106.4(ACVR2B):c.*394G>A rs115298793 0.00292
NM_001106.4(ACVR2B):c.*5700A>C rs141178727 0.00261
NM_001106.4(ACVR2B):c.*4218A>G rs146770581 0.00253
NM_001106.4(ACVR2B):c.*15T>C rs45457192 0.00156
NM_001106.4(ACVR2B):c.*8026C>T rs139304868 0.00139
NM_001106.4(ACVR2B):c.*133A>T rs186832239 0.00135
NM_001106.4(ACVR2B):c.*2005C>T rs573846950 0.00115
NM_001106.4(ACVR2B):c.*427C>G rs543992989 0.00091
NM_001106.4(ACVR2B):c.*7413T>C rs148351980 0.00091
NM_001106.4(ACVR2B):c.*483C>T rs189885640 0.00069
NM_001106.4(ACVR2B):c.*6156C>T rs184122552 0.00059
NM_001106.4(ACVR2B):c.*4423A>G rs184076956 0.00052
NM_001106.4(ACVR2B):c.*1429C>T rs188712951 0.00040
NM_001106.4(ACVR2B):c.*7619C>T rs563606458 0.00021
NM_001106.4(ACVR2B):c.*3334G>T rs557881549 0.00019
NM_001106.4(ACVR2B):c.*420A>G rs556691662 0.00017
NM_001106.4(ACVR2B):c.*3570A>G rs528466104 0.00014
NM_001106.4(ACVR2B):c.*5901C>T rs191838801 0.00011
NM_001106.4(ACVR2B):c.*6638C>T rs552937102 0.00004
NM_001106.4(ACVR2B):c.147C>T (p.Cys49=) rs201686292 0.00004
NM_001106.4(ACVR2B):c.*3169T>A rs149804558 0.00002
NM_001106.4(ACVR2B):c.*1376G>A rs369336725 0.00001
NM_001106.4(ACVR2B):c.*1041A>C rs7640050
NM_001106.4(ACVR2B):c.*1346_*1347del rs397989264
NM_001106.4(ACVR2B):c.*1891G>C rs541955988
NM_001106.4(ACVR2B):c.*3714G>T rs928813
NM_001106.4(ACVR2B):c.*6388T>G rs7374458
NM_001106.4(ACVR2B):c.*9318dup rs150324551

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