ClinVar Miner

List of variants in gene ADAMTS13 studied for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 159
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HGVS dbSNP
NC_000009.12:g.133422276C>T
NC_000009.12:g.133422418C>T
NC_000009.12:g.133422458C>T
NC_000009.12:g.133423131G>A
NC_000009.12:g.133424379C>T
NC_000009.12:g.133425571C>T
NC_000009.12:g.133426068C>T
NC_000009.12:g.133426205C>T
NC_000009.12:g.133428662G>A
NC_000009.12:g.133428763C>G
NC_000009.12:g.133428779C>T
NC_000009.12:g.133430019G>A
NC_000009.12:g.133433441C>T
NC_000009.12:g.133433442G>A
NC_000009.12:g.133436912C>T
NC_000009.12:g.133437750G>A
NC_000009.12:g.133437831C>A
NC_000009.12:g.133439362C>T
NC_000009.12:g.133439363T>A
NC_000009.12:g.133440336C>G
NC_000009.12:g.133440388A>G
NC_000009.12:g.133440435C>T
NC_000009.12:g.133440468G>T
NC_000009.12:g.133440473G>A
NC_000009.12:g.133442519G>A
NC_000009.12:g.133443506G>A
NC_000009.12:g.133444951G>A
NC_000009.12:g.133444987G>A
NC_000009.12:g.133448694C>T
NC_000009.12:g.133448728G>A
NC_000009.12:g.133449811G>A
NC_000009.12:g.133449833T>C
NC_000009.12:g.133454537C>T
NC_000009.12:g.133454549G>A
NC_000009.12:g.133455454C>T
NC_000009.12:g.133455458C>T
NC_000009.12:g.133455467C>T
NC_000009.12:g.133455571T>A
NC_000009.12:g.133456185G>A
NC_000009.12:g.133456190T>A
NC_000009.12:g.133456213C>T
NC_000009.12:g.133456568G>C
NC_000009.12:g.133456652C>T
NC_000009.12:g.133457973C>T
NC_000009.12:g.133457979A>G
NC_000009.12:g.133459020A>G
NC_000009.12:g.133459081G>A
NC_000009.12:g.133459084G>T
NC_000009.12:g.133459221G>A
NC_000009.12:g.133459257C>T
NC_000009.12:g.133459348C>T
NM_139025.3(ADAMTS13):c.[1342C>G;1523G>A]
NM_139025.4(ADAMTS13):c.-155C>T rs587712950
NM_139025.4(ADAMTS13):c.-280G>A rs777585429
NM_139025.4(ADAMTS13):c.-357T>C rs34265876
NM_139025.4(ADAMTS13):c.-52C>G rs587771364
NM_139025.4(ADAMTS13):c.1022C>T (p.Pro341Leu)
NM_139025.4(ADAMTS13):c.1193G>A (p.Arg398His) rs121908471
NM_139025.4(ADAMTS13):c.1200C>T (p.Cys400=)
NM_139025.4(ADAMTS13):c.1245-3C>T rs36219902
NM_139025.4(ADAMTS13):c.1341G>A (p.Ser447=) rs587602874
NM_139025.4(ADAMTS13):c.1342C>G (p.Gln448Glu) rs2301612
NM_139025.4(ADAMTS13):c.1345C>T (p.Gln449Ter) rs121908476
NM_139025.4(ADAMTS13):c.1359C>T (p.Thr453=) rs148365271
NM_139025.4(ADAMTS13):c.1368G>T (p.Gln456His) rs36220239
NM_139025.4(ADAMTS13):c.1370C>T (p.Pro457Leu) rs36220240
NM_139025.4(ADAMTS13):c.1423C>T (p.Pro475Ser) rs11575933
NM_139025.4(ADAMTS13):c.1435+11C>T rs377454829
NM_139025.4(ADAMTS13):c.1551G>C (p.Gly517=) rs148472763
NM_139025.4(ADAMTS13):c.1582A>G (p.Arg528Gly) rs121908473
NM_139025.4(ADAMTS13):c.1584+5G>A rs782235228
NM_139025.4(ADAMTS13):c.1585-1G>C rs1554789680
NM_139025.4(ADAMTS13):c.1783_1784del (p.Leu595fs) rs387906344
NM_139025.4(ADAMTS13):c.1787-6C>T rs781938740
NM_139025.4(ADAMTS13):c.1787C>T (p.Ala596Val) rs281875299
NM_139025.4(ADAMTS13):c.1797C>T (p.Ile599=) rs36221216
NM_139025.4(ADAMTS13):c.1830C>T (p.Ser610=) rs36221217
NM_139025.4(ADAMTS13):c.1841A>C (p.Asn614Thr) rs782396358
NM_139025.4(ADAMTS13):c.1852C>G (p.Pro618Ala) rs28647808
NM_139025.4(ADAMTS13):c.1874G>A (p.Arg625His) rs36090624
NM_139025.4(ADAMTS13):c.1930C>T (p.Arg644Cys) rs782659882
NM_139025.4(ADAMTS13):c.19C>T (p.Arg7Trp) rs34024143
NM_139025.4(ADAMTS13):c.2017A>T (p.Ile673Phe) rs281875307
NM_139025.4(ADAMTS13):c.2074C>T (p.Arg692Cys) rs121908475
NM_139025.4(ADAMTS13):c.2107C>T (p.Leu703=) rs146314458
NM_139025.4(ADAMTS13):c.2167C>A (p.Gln723Lys) rs138014548
NM_139025.4(ADAMTS13):c.2209T>C (p.Cys737Arg) rs1554791280
NM_139025.4(ADAMTS13):c.2217C>T (p.Leu739=) rs144178018
NM_139025.4(ADAMTS13):c.2218G>A (p.Glu740Lys) rs36221451
NM_139025.4(ADAMTS13):c.2308G>A (p.Val770Met) rs374606481
NM_139025.4(ADAMTS13):c.2376_2401del (p.Ala793fs) rs387906342
NM_139025.4(ADAMTS13):c.2494G>A (p.Val832Met)
NM_139025.4(ADAMTS13):c.2508T>C (p.Asp836=) rs36221472
NM_139025.4(ADAMTS13):c.2580C>T (p.Val860=) rs147112200
NM_139025.4(ADAMTS13):c.262G>A (p.Val88Met) rs281875302
NM_139025.4(ADAMTS13):c.2699C>T (p.Ala900Val) rs685523
NM_139025.4(ADAMTS13):c.2708C>T (p.Ser903Leu) rs78977446
NM_139025.4(ADAMTS13):c.2732-8C>T rs886063634
NM_139025.4(ADAMTS13):c.2851T>G (p.Cys951Gly) rs121908468
NM_139025.4(ADAMTS13):c.2863dup (p.Trp955fs)
NM_139025.4(ADAMTS13):c.286C>G (p.His96Asp) rs121908467
NM_139025.4(ADAMTS13):c.2910C>T (p.Val970=) rs28641026
NM_139025.4(ADAMTS13):c.2915G>A (p.Arg972Gln) rs139951127
NM_139025.4(ADAMTS13):c.291_319del (p.Glu98fs) rs387906345
NM_139025.4(ADAMTS13):c.2931_2936del (p.Cys977_Arg979delinsTrp) rs387906346
NM_139025.4(ADAMTS13):c.2935del (p.Arg979fs) rs886063635
NM_139025.4(ADAMTS13):c.3044+10C>T rs375335095
NM_139025.4(ADAMTS13):c.3044+8A>C rs886063636
NM_139025.4(ADAMTS13):c.304C>T (p.Arg102Cys) rs121908469
NM_139025.4(ADAMTS13):c.3070T>G (p.Cys1024Gly) rs121908472
NM_139025.4(ADAMTS13):c.3097G>A (p.Ala1033Thr) rs28503257
NM_139025.4(ADAMTS13):c.3108G>A (p.Ser1036=) rs34934621
NM_139025.4(ADAMTS13):c.3153C>T (p.Asp1051=) rs782748173
NM_139025.4(ADAMTS13):c.3159G>A (p.Ala1053=) rs200349242
NM_139025.4(ADAMTS13):c.3178C>T (p.Arg1060Trp) rs142572218
NM_139025.4(ADAMTS13):c.3287G>A (p.Arg1096His) rs61751476
NM_139025.4(ADAMTS13):c.330+1G>A rs375415632
NM_139025.4(ADAMTS13):c.331-1G>A rs786205078
NM_139025.4(ADAMTS13):c.3348G>A (p.Leu1116=) rs146073007
NM_139025.4(ADAMTS13):c.3417G>T (p.Val1139=) rs782724202
NM_139025.4(ADAMTS13):c.3445C>T (p.Arg1149Trp)
NM_139025.4(ADAMTS13):c.3541G>A (p.Gly1181Arg) rs192619276
NM_139025.4(ADAMTS13):c.354G>A (p.Pro118=) rs28571612
NM_139025.4(ADAMTS13):c.357C>T (p.Ser119=) rs147563206
NM_139025.4(ADAMTS13):c.3638G>A (p.Cys1213Tyr) rs121908474
NM_139025.4(ADAMTS13):c.3651T>C (p.Ile1217=) rs782235608
NM_139025.4(ADAMTS13):c.3663C>T (p.Leu1221=) rs144916851
NM_139025.4(ADAMTS13):c.3677C>T (p.Thr1226Ile)
NM_139025.4(ADAMTS13):c.3770dup (p.Leu1258fs) rs387906341
NM_139025.4(ADAMTS13):c.3796A>T (p.Thr1266Ser) rs782798764
NM_139025.4(ADAMTS13):c.3826G>A (p.Gly1276Arg) rs144808448
NM_139025.4(ADAMTS13):c.3846G>A (p.Val1282=) rs36222899
NM_139025.4(ADAMTS13):c.3941C>T (p.Ser1314Leu) rs142060916
NM_139025.4(ADAMTS13):c.4109C>T (p.Ala1370Val) rs782145338
NM_139025.4(ADAMTS13):c.414+1G>A rs786205077
NM_139025.4(ADAMTS13):c.4143dup (p.Glu1382fs) rs387906343
NM_139025.4(ADAMTS13):c.415-1G>A
NM_139025.4(ADAMTS13):c.415-5C>T rs200230025
NM_139025.4(ADAMTS13):c.4221C>A (p.Thr1407=) rs1055432
NM_139025.4(ADAMTS13):c.460G>A (p.Val154Ile) rs369026148
NM_139025.4(ADAMTS13):c.539+7G>A rs184864675
NM_139025.4(ADAMTS13):c.540-3G>A rs886063631
NM_139025.4(ADAMTS13):c.559G>C (p.Asp187His) rs148312697
NM_139025.4(ADAMTS13):c.577C>T (p.Arg193Trp) rs281875287
NM_139025.4(ADAMTS13):c.581G>T (p.Gly194Val) rs1554785242
NM_139025.4(ADAMTS13):c.582C>T (p.Gly194=) rs34054981
NM_139025.4(ADAMTS13):c.587C>T (p.Thr196Ile) rs121908470
NM_139025.4(ADAMTS13):c.686+4T>G rs36219245
NM_139025.4(ADAMTS13):c.749C>T (p.Ala250Val) rs121908478
NM_139025.4(ADAMTS13):c.775G>A (p.Gly259Ser) rs886063632
NM_139025.4(ADAMTS13):c.803G>C (p.Arg268Pro) rs121908477
NM_139025.4(ADAMTS13):c.824+12C>T rs587678724
NM_139025.4(ADAMTS13):c.824+13C>T rs149586801
NM_139025.4(ADAMTS13):c.824+5C>G rs886063633
NM_139025.4(ADAMTS13):c.870C>T (p.Pro290=) rs754541465
NM_139025.4(ADAMTS13):c.936C>T (p.Arg312=) rs36219562
NM_139025.4(ADAMTS13):c.987+11C>T rs28729234
NM_139026.5(ADAMTS13):c.3307+143del rs1060499780
NM_139026.5(ADAMTS13):c.3844_3960del (p.Thr1282_Thr1320del) rs1554797078

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