ClinVar Miner

List of variants reported as benign for Wagner disease by Illumina Laboratory Services, Illumina

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_004385.5(VCAN):c.9882C>T (p.Val3294=) rs308365 0.97301
NM_004385.5(VCAN):c.4323G>A (p.Gln1441=) rs2548541 0.67722
NM_004385.5(VCAN):c.*1429A>G rs11726 0.54953
NM_004385.5(VCAN):c.4547A>G (p.Lys1516Arg) rs309559 0.50554
NM_004385.5(VCAN):c.5808T>C (p.Gly1936=) rs309557 0.50487
NM_004385.5(VCAN):c.6723A>G (p.Arg2241=) rs160279 0.50384
NM_004385.5(VCAN):c.348T>C (p.Thr116=) rs12332199 0.40199
NM_004385.5(VCAN):c.5477G>A (p.Arg1826His) rs188703 0.38473
NM_004385.5(VCAN):c.645A>G (p.Val215=) rs4470745 0.33601
NM_004385.5(VCAN):c.1283G>A (p.Gly428Asp) rs2287926 0.16841
NM_004385.5(VCAN):c.*1436C>T rs15071 0.16029
NM_004385.5(VCAN):c.*1601T>A rs1050948 0.13706
NM_004385.5(VCAN):c.9379+7T>C rs695103 0.09623
NM_004385.5(VCAN):c.4569A>G (p.Thr1523=) rs16900528 0.06757
NM_004385.5(VCAN):c.9630C>T (p.His3210=) rs16900564 0.05374
NM_004385.5(VCAN):c.9033C>A (p.Asn3011Lys) rs16900532 0.05068
NM_004385.5(VCAN):c.*730A>G rs8061 0.03976
NM_004385.5(VCAN):c.7030C>T (p.Pro2344Ser) rs61733401 0.02963
NM_004385.5(VCAN):c.9075G>A (p.Thr3025=) rs113014073 0.02820
NM_004385.5(VCAN):c.1043-10A>G rs115912456 0.02772
NM_004385.5(VCAN):c.1045A>G (p.Lys349Glu) rs61749613 0.02772
NM_004385.5(VCAN):c.8090G>A (p.Arg2697His) rs61733389 0.02711
NM_004385.5(VCAN):c.393C>T (p.Asp131=) rs35042106 0.01920
NM_004385.5(VCAN):c.426G>A (p.Thr142=) rs35031282 0.01806
NM_004385.5(VCAN):c.5155A>T (p.Thr1719Ser) rs113965318 0.01319
NM_004385.5(VCAN):c.5576C>A (p.Ala1859Glu) rs34050047 0.01316
NM_004385.5(VCAN):c.*1603T>C rs10233 0.01297
NM_004385.5(VCAN):c.6123C>T (p.Ile2041=) rs113659987 0.01282
NM_004385.5(VCAN):c.6237G>A (p.Lys2079=) rs80200229 0.01278
NM_004385.5(VCAN):c.8622G>A (p.Ala2874=) rs3096171 0.01237
NM_004385.5(VCAN):c.899C>T (p.Ser300Leu) rs2652098 0.00988
NM_004385.5(VCAN):c.4422T>C (p.Thr1474=) rs61733395 0.00980
NM_004385.5(VCAN):c.9104C>T (p.Ala3035Val) rs111512368 0.00955
NM_004385.5(VCAN):c.*1678G>T rs10411 0.00929
NM_004385.5(VCAN):c.2065A>G (p.Thr689Ala) rs61754531 0.00895
NM_004385.5(VCAN):c.7419C>T (p.Ser2473=) rs61754536 0.00819
NM_004385.5(VCAN):c.2378T>C (p.Leu793Ser) rs76165877 0.00793
NM_004385.5(VCAN):c.2887C>T (p.Pro963Ser) rs76914270 0.00597
NM_004385.5(VCAN):c.*910A>C rs201146484 0.00164
NM_004385.5(VCAN):c.7743T>C (p.Asp2581=) rs75771891 0.00160
NM_004385.5(VCAN):c.2668G>T (p.Gly890Cys) rs146527005 0.00088
NM_004385.5(VCAN):c.4643C>T (p.Ser1548Leu) rs61754534 0.00030
NM_004385.5(VCAN):c.9758A>G (p.Asn3253Ser) rs141195210 0.00022
NM_004385.5(VCAN):c.160C>T (p.Pro54Ser) rs140063016 0.00019
NM_004385.5(VCAN):c.6322C>G (p.Gln2108Glu) rs62364883 0.00017
NM_004385.5(VCAN):c.221A>G (p.Asn74Ser) rs144766017 0.00016
NM_004385.5(VCAN):c.1369G>A (p.Glu457Lys) rs145029761 0.00015
NM_004385.5(VCAN):c.157C>T (p.Pro53Ser) rs201466502 0.00014
NM_004385.5(VCAN):c.1896G>A (p.Thr632=) rs377633742 0.00012
NM_004385.5(VCAN):c.2925T>C (p.Leu975=) rs139028655 0.00012
NM_004385.5(VCAN):c.5489C>T (p.Ser1830Phe) rs141725839 0.00011
NM_004385.5(VCAN):c.8089C>T (p.Arg2697Cys) rs146336600 0.00011
NM_004385.5(VCAN):c.*1081C>T rs78087172 0.00010
NM_004385.5(VCAN):c.6649C>T (p.Pro2217Ser) rs139730890 0.00010
NM_004385.5(VCAN):c.7371C>T (p.Thr2457=) rs199626605 0.00008
NM_004385.5(VCAN):c.9454C>G (p.Leu3152Val) rs183984308 0.00007
NM_004385.5(VCAN):c.*1296A>G rs572066915 0.00006
NM_004385.5(VCAN):c.329T>G (p.Val110Gly) rs750836310 0.00006
NM_004385.5(VCAN):c.*672A>G rs532790573 0.00005
NM_004385.5(VCAN):c.*89A>G rs369600306 0.00005
NM_004385.5(VCAN):c.9009G>A (p.Thr3003=) rs200462738 0.00004
NM_004385.5(VCAN):c.9619A>G (p.Ile3207Val) rs763005838 0.00004
NM_004385.5(VCAN):c.1457C>T (p.Ser486Leu) rs186544077 0.00003
NM_004385.5(VCAN):c.5681T>C (p.Val1894Ala) rs780104369 0.00002
NM_004385.5(VCAN):c.7999G>C (p.Gly2667Arg) rs774497812 0.00002
NM_004385.5(VCAN):c.909C>T (p.Ser303=) rs754375176 0.00001
NM_004385.5(VCAN):c.*1548del rs397998455
NM_004385.5(VCAN):c.*1717C>A rs537687030
NM_004385.5(VCAN):c.1009C>G (p.Pro337Ala) rs199827515
NM_004385.5(VCAN):c.1650C>T (p.Phe550=) rs532077063
NM_004385.5(VCAN):c.630C>T (p.Ile210=) rs538498172
NM_004385.5(VCAN):c.6902T>A (p.Phe2301Tyr) rs160278
NM_004385.5(VCAN):c.8809G>T (p.Asp2937Tyr) rs160277
NM_004385.5(VCAN):c.927T>C (p.Thr309=) rs536465380

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