ClinVar Miner

List of variants in gene ADAMTS13 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_139025.4(ADAMTS13):c.-155C>T rs587712950
NM_139025.4(ADAMTS13):c.-280G>A rs777585429
NM_139025.4(ADAMTS13):c.-52C>G rs587771364
NM_139025.4(ADAMTS13):c.1245-3C>T rs36219902
NM_139025.4(ADAMTS13):c.1341G>A (p.Ser447=) rs587602874
NM_139025.4(ADAMTS13):c.1359C>T (p.Thr453=) rs148365271
NM_139025.4(ADAMTS13):c.1435+11C>T rs377454829
NM_139025.4(ADAMTS13):c.1551G>C (p.Gly517=) rs148472763
NM_139025.4(ADAMTS13):c.1787-6C>T rs781938740
NM_139025.4(ADAMTS13):c.1830C>T (p.Ser610=) rs36221217
NM_139025.4(ADAMTS13):c.1930C>T (p.Arg644Cys) rs782659882
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.2217C>T (p.Leu739=) rs144178018
NM_139025.4(ADAMTS13):c.2308G>A (p.Val770Met) rs374606481
NM_139025.4(ADAMTS13):c.2580C>T (p.Val860=) rs147112200
NM_139025.4(ADAMTS13):c.2732-8C>T rs886063634
NM_139025.4(ADAMTS13):c.2915G>A (p.Arg972Gln) rs139951127
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.3153C>T (p.Asp1051=) rs782748173
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.3651T>C (p.Ile1217=) rs782235608
NM_139025.4(ADAMTS13):c.3663C>T (p.Leu1221=) rs144916851
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.4109C>T (p.Ala1370Val) rs782145338
NM_139025.4(ADAMTS13):c.415-5C>T rs200230025
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.775G>A (p.Gly259Ser) rs886063632
NM_139025.4(ADAMTS13):c.824+12C>T rs587678724
NM_139025.4(ADAMTS13):c.824+5C>G rs886063633
NM_139025.4(ADAMTS13):c.870C>T (p.Pro290=) rs754541465

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