ClinVar Miner

List of variants in gene ADAMTS2 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP
NM_014244.5(ADAMTS2):c.*1361A>G rs142875628
NM_014244.5(ADAMTS2):c.*1446dup rs151062906
NM_014244.5(ADAMTS2):c.*1573A>C rs560216364
NM_014244.5(ADAMTS2):c.*1639C>T rs138971097
NM_014244.5(ADAMTS2):c.*1747A>C rs886060486
NM_014244.5(ADAMTS2):c.*1797C>T rs553329835
NM_014244.5(ADAMTS2):c.*181C>T rs886060489
NM_014244.5(ADAMTS2):c.*183T>C rs184732586
NM_014244.5(ADAMTS2):c.*1919T>G rs574968586
NM_014244.5(ADAMTS2):c.*1941C>T rs886060485
NM_014244.5(ADAMTS2):c.*2064A>G rs759155545
NM_014244.5(ADAMTS2):c.*2147C>T rs886060484
NM_014244.5(ADAMTS2):c.*222C>T rs886060488
NM_014244.5(ADAMTS2):c.*2270C>T rs886060483
NM_014244.5(ADAMTS2):c.*2440G>A rs546192004
NM_014244.5(ADAMTS2):c.*2587T>C rs140304884
NM_014244.5(ADAMTS2):c.*2589T>G rs886060482
NM_014244.5(ADAMTS2):c.*2595C>T rs188054405
NM_014244.5(ADAMTS2):c.*2598A>G rs371733200
NM_014244.5(ADAMTS2):c.*2724A>G rs886060481
NM_014244.5(ADAMTS2):c.*2853G>A rs565652629
NM_014244.5(ADAMTS2):c.*2854T>C rs11740156
NM_014244.5(ADAMTS2):c.*288G>A rs59090242
NM_014244.5(ADAMTS2):c.*2923_*2925AAC[1] rs886060480
NM_014244.5(ADAMTS2):c.*2951_*2952delinsAA rs386695575
NM_014244.5(ADAMTS2):c.*353C>T rs886060487
NM_014244.5(ADAMTS2):c.*445G>A rs73806886
NM_014244.5(ADAMTS2):c.*707A>G rs149592164
NM_014244.5(ADAMTS2):c.*816C>T rs116130524
NM_014244.5(ADAMTS2):c.*843G>A rs778909760
NM_014244.5(ADAMTS2):c.*977G>A rs138084603
NM_014244.5(ADAMTS2):c.-13C>A rs886060499
NM_014244.5(ADAMTS2):c.-45T>C rs886060500
NM_014244.5(ADAMTS2):c.1069G>A (p.Asp357Asn) rs763890617
NM_014244.5(ADAMTS2):c.1123G>A (p.Gly375Ser) rs886060494
NM_014244.5(ADAMTS2):c.1164G>A (p.Pro388=) rs141348218
NM_014244.5(ADAMTS2):c.1308G>A (p.Ala436=) rs41285549
NM_014244.5(ADAMTS2):c.1431G>A (p.Ala477=) rs147259971
NM_014244.5(ADAMTS2):c.1458C>T (p.Tyr486=) rs61757478
NM_014244.5(ADAMTS2):c.1644A>G (p.Gly548=) rs61731454
NM_014244.5(ADAMTS2):c.1883G>A (p.Arg628His) rs140621260
NM_014244.5(ADAMTS2):c.2015G>T (p.Arg672Leu) rs200806292
NM_014244.5(ADAMTS2):c.2036G>T (p.Arg679Leu) rs144554943
NM_014244.5(ADAMTS2):c.2073C>T (p.Arg691=) rs149391669
NM_014244.5(ADAMTS2):c.2109C>T (p.Ile703=) rs200210415
NM_014244.5(ADAMTS2):c.2145C>T (p.Cys715=) rs372661052
NM_014244.5(ADAMTS2):c.2172G>C (p.Val724=) rs150587776
NM_014244.5(ADAMTS2):c.220G>A (p.Val74Met) rs2271211
NM_014244.5(ADAMTS2):c.2276C>A (p.Thr759Asn) rs886060493
NM_014244.5(ADAMTS2):c.2290+15C>T rs764259203
NM_014244.5(ADAMTS2):c.2292C>T (p.Ala764=) rs188566209
NM_014244.5(ADAMTS2):c.2382G>A (p.Glu794=) rs745407557
NM_014244.5(ADAMTS2):c.2439C>T (p.His813=) rs141661592
NM_014244.5(ADAMTS2):c.258C>G (p.Ala86=) rs886060497
NM_014244.5(ADAMTS2):c.2727C>T (p.Asn909=) rs151261888
NM_014244.5(ADAMTS2):c.2751-4G>A rs112155474
NM_014244.5(ADAMTS2):c.2797A>G (p.Thr933Ala) rs886060492
NM_014244.5(ADAMTS2):c.2811G>A (p.Val937=) rs557019144
NM_014244.5(ADAMTS2):c.2817C>T (p.Ser939=) rs201215425
NM_014244.5(ADAMTS2):c.2818G>A (p.Val940Met) rs367796431
NM_014244.5(ADAMTS2):c.2834C>T (p.Pro945Leu) rs200309353
NM_014244.5(ADAMTS2):c.2914C>T (p.Arg972Cys) rs867846785
NM_014244.5(ADAMTS2):c.2980G>A (p.Gly994Ser) rs142429109
NM_014244.5(ADAMTS2):c.3078C>T (p.Gly1026=) rs886060491
NM_014244.5(ADAMTS2):c.3342C>T (p.Asn1114=) rs79606317
NM_014244.5(ADAMTS2):c.3351C>T (p.Asp1117=) rs777279065
NM_014244.5(ADAMTS2):c.3367C>T (p.Leu1123Phe) rs201343773
NM_014244.5(ADAMTS2):c.3423G>A (p.Glu1141=) rs886060490
NM_014244.5(ADAMTS2):c.3449A>G (p.Asn1150Ser) rs200982805
NM_014244.5(ADAMTS2):c.3506G>T (p.Gly1169Val) rs117187367
NM_014244.5(ADAMTS2):c.447G>A (p.Glu149=) rs886060496
NM_014244.5(ADAMTS2):c.661C>G (p.Leu221Val) rs756807336
NM_014244.5(ADAMTS2):c.669G>T (p.Gly223=) rs886060495
NM_014244.5(ADAMTS2):c.710A>C (p.Asp237Ala) rs202197821
NM_014244.5(ADAMTS2):c.724G>A (p.Ala242Thr) rs372103269
NM_014244.5(ADAMTS2):c.748G>A (p.Ala250Thr) rs143764421
NM_014244.5(ADAMTS2):c.764G>A (p.Arg255Gln) rs117222015
NM_014244.5(ADAMTS2):c.784G>A (p.Ala262Thr) rs376820857
NM_014244.5(ADAMTS2):c.95C>T (p.Pro32Leu) rs886060498
NM_014244.5(ADAMTS2):c.991G>A (p.Glu331Lys) rs17667857

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