ClinVar Miner

List of variants in gene ADAMTS2 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
Download table as spreadsheet
HGVS dbSNP
NM_014244.5(ADAMTS2):c.-13C>A rs886060499
NM_014244.5(ADAMTS2):c.-33C>T rs1057523882
NM_014244.5(ADAMTS2):c.110C>T (p.Ala37Val) rs1057524401
NM_014244.5(ADAMTS2):c.1122C>T (p.Ser374=) rs145109914
NM_014244.5(ADAMTS2):c.115C>T (p.Leu39Phe) rs1064796637
NM_014244.5(ADAMTS2):c.1373G>A (p.Arg458His) rs768230986
NM_014244.5(ADAMTS2):c.142G>C (p.Gly48Arg) rs769371687
NM_014244.5(ADAMTS2):c.1430C>T (p.Ala477Val) rs370614125
NM_014244.5(ADAMTS2):c.1488C>T (p.Phe496=) rs147438064
NM_014244.5(ADAMTS2):c.1511C>T (p.Thr504Met) rs765595538
NM_014244.5(ADAMTS2):c.1816G>A (p.Asp606Asn) rs138399615
NM_014244.5(ADAMTS2):c.1867C>T (p.Arg623Cys) rs752401488
NM_014244.5(ADAMTS2):c.1869C>T (p.Arg623=) rs376058580
NM_014244.5(ADAMTS2):c.2237C>T (p.Ala746Val) rs780147082
NM_014244.5(ADAMTS2):c.2272G>A (p.Ala758Thr) rs146222244
NM_014244.5(ADAMTS2):c.2558C>G (p.Ser853Cys) rs1057521585
NM_014244.5(ADAMTS2):c.260G>T (p.Arg87Leu)
NM_014244.5(ADAMTS2):c.2674C>T (p.Arg892Cys) rs1554123906
NM_014244.5(ADAMTS2):c.2751-4G>A rs112155474
NM_014244.5(ADAMTS2):c.2780G>A (p.Ser927Asn) rs1193602528
NM_014244.5(ADAMTS2):c.2818G>A (p.Val940Met) rs367796431
NM_014244.5(ADAMTS2):c.2842_2844del (p.Asp948del) rs765659887
NM_014244.5(ADAMTS2):c.3038A>C (p.Gln1013Pro) rs371013989
NM_014244.5(ADAMTS2):c.3076G>A (p.Gly1026Ser) rs148344708
NM_014244.5(ADAMTS2):c.3178+4A>G rs948167718
NM_014244.5(ADAMTS2):c.3343G>A (p.Asp1115Asn) rs200022037
NM_014244.5(ADAMTS2):c.3551C>T (p.Pro1184Leu) rs150989902
NM_014244.5(ADAMTS2):c.3625G>A (p.Gly1209Arg) rs769813298
NM_014244.5(ADAMTS2):c.547C>T (p.Arg183Trp) rs372225444
NM_014244.5(ADAMTS2):c.640C>T (p.Arg214Trp) rs144732073
NM_014244.5(ADAMTS2):c.655C>T (p.Pro219Ser) rs146217716
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.773G>A (p.Arg258His) rs1057524562
NM_014244.5(ADAMTS2):c.784G>A (p.Ala262Thr) rs376820857
NM_014244.5(ADAMTS2):c.80_100dup (p.Leu27_Pro33dup) rs1064794627
NM_014244.5(ADAMTS2):c.847G>A (p.Gly283Arg) rs376856341
NM_014244.5(ADAMTS2):c.94C>T (p.Pro32Ser) rs547548078
NM_014244.5(ADAMTS2):c.991G>A (p.Glu331Lys) rs17667857
NM_014244.5(ADAMTS2):c.997G>A (p.Gly333Arg) rs483352736

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.