ClinVar Miner

List of variants in gene DOCK2 reported as benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_004946.3(DOCK2):c.2727G>A (p.Gln909=) rs261623 0.46437
NM_004946.3(DOCK2):c.3612C>T (p.Thr1204=) rs3763048 0.42784
NM_004946.3(DOCK2):c.3468-4G>A rs3763047 0.41818
NM_004946.3(DOCK2):c.3456C>G (p.Leu1152=) rs9791113 0.40563
NM_004946.3(DOCK2):c.1374A>G (p.Lys458=) rs2306559 0.37207
NM_004946.3(DOCK2):c.4896T>C (p.Arg1632=) rs1045168 0.32381
NM_004946.3(DOCK2):c.1259-23G>A rs2306560 0.25632
NM_004946.3(DOCK2):c.3195A>C (p.Leu1065=) rs2287727 0.23497
NM_004946.3(DOCK2):c.1212C>A (p.Thr404=) rs2112703 0.16933
NM_004946.3(DOCK2):c.3828G>C (p.Leu1276=) rs6555882 0.09317
NM_004946.3(DOCK2):c.2133-13A>T rs80250373 0.05819
NM_004946.3(DOCK2):c.843+7G>A rs72841138 0.04984
NM_004946.3(DOCK2):c.2352A>G (p.Gln784=) rs13155521 0.04295
NM_004946.3(DOCK2):c.2946G>A (p.Lys982=) rs36028557 0.01626
NM_004946.3(DOCK2):c.366C>T (p.Tyr122=) rs35393134 0.01566
NM_004946.3(DOCK2):c.4314C>T (p.Tyr1438=) rs17647491 0.01462
NM_004946.3(DOCK2):c.752C>T (p.Thr251Met) rs78243868 0.01316
NM_004946.3(DOCK2):c.2241T>C (p.Ile747=) rs35887608 0.01082
NM_004946.3(DOCK2):c.3945T>C (p.Tyr1315=) rs34133853 0.00985
NM_004946.3(DOCK2):c.5344C>T (p.Arg1782Cys) rs149343589 0.00820
NM_004946.3(DOCK2):c.1483-17dup rs149389326 0.00768
NM_004946.3(DOCK2):c.2199C>T (p.Ile733=) rs35530753 0.00761
NM_004946.3(DOCK2):c.5475G>A (p.Ser1825=) rs114098294 0.00570
NM_004946.3(DOCK2):c.4729-4C>T rs115841644 0.00479
NM_004946.3(DOCK2):c.3192G>T (p.Arg1064=) rs58980222 0.00472
NM_004946.3(DOCK2):c.4295+9C>T rs115134653 0.00358
NM_004946.3(DOCK2):c.4976G>C (p.Ser1659Thr) rs139644615 0.00333
NM_004946.3(DOCK2):c.4955A>G (p.Asn1652Ser) rs113216049 0.00320
NM_004946.3(DOCK2):c.631A>G (p.Met211Val) rs151191554 0.00305
NM_004946.3(DOCK2):c.3966+13C>T rs188426806 0.00237
NM_004946.3(DOCK2):c.1383+12A>G rs182075506 0.00226
NM_004946.3(DOCK2):c.279G>T (p.Thr93=) rs144632263 0.00201
NM_004946.3(DOCK2):c.3624+16G>A rs113020462 0.00180
NM_004946.3(DOCK2):c.3417G>A (p.Glu1139=) rs149853735 0.00144
NM_004946.3(DOCK2):c.753G>A (p.Thr251=) rs146746458 0.00113
NM_004946.3(DOCK2):c.3414C>T (p.His1138=) rs148138145 0.00110
NM_004946.3(DOCK2):c.5484G>A (p.Thr1828=) rs140198889 0.00095
NM_004946.3(DOCK2):c.5335A>T (p.Thr1779Ser) rs2270898 0.00092
NM_004946.3(DOCK2):c.5445G>A (p.Ser1815=) rs200128185 0.00090
NM_004946.3(DOCK2):c.640C>T (p.Arg214Trp) rs150969388 0.00063
NM_004946.3(DOCK2):c.1062A>G (p.Thr354=) rs143288655 0.00055
NM_004946.3(DOCK2):c.4854T>C (p.Gly1618=) rs2270900 0.00045
NM_004946.3(DOCK2):c.264A>G (p.Ala88=) rs201493926 0.00020
NM_004946.3(DOCK2):c.4295+10G>A rs200461316 0.00020
NM_004946.3(DOCK2):c.5295G>A (p.Ala1765=) rs370911923 0.00018
NM_004946.3(DOCK2):c.2106G>A (p.Gln702=) rs75416239 0.00016
NM_004946.3(DOCK2):c.2898+18T>C rs201529422 0.00016
NM_004946.3(DOCK2):c.2448-17A>G rs201930456 0.00011
NM_004946.3(DOCK2):c.4728+11G>A rs376343917 0.00009
NM_004946.3(DOCK2):c.1417A>G (p.Met473Val) rs201626676 0.00006
NM_004946.3(DOCK2):c.5024C>T (p.Thr1675Met) rs201322810 0.00006
NM_004946.3(DOCK2):c.5476C>T (p.Leu1826=) rs550039123 0.00001
NM_004946.3(DOCK2):c.1056-10dup
NM_004946.3(DOCK2):c.169-72G>C rs2306564
NM_004946.3(DOCK2):c.1767T>C (p.Val589=) rs34864600
NM_004946.3(DOCK2):c.1767T>G (p.Val589=) rs34864600
NM_004946.3(DOCK2):c.3073-8A>G rs113289730
NM_004946.3(DOCK2):c.3381+8del rs1755634287

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