ClinVar Miner

List of variants in gene ADAMTS2 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 30
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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.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.1816G>A (p.Asp606Asn) rs138399615
NM_014244.5(ADAMTS2):c.1867C>T (p.Arg623Cys) rs752401488
NM_014244.5(ADAMTS2):c.1883G>A (p.Arg628His) rs140621260
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.2674C>T (p.Arg892Cys) rs1554123906
NM_014244.5(ADAMTS2):c.2780G>A (p.Ser927Asn) rs1193602528
NM_014244.5(ADAMTS2):c.2795G>A (p.Arg932Gln) rs140022033
NM_014244.5(ADAMTS2):c.2842_2844del (p.Asp948del) rs765659887
NM_014244.5(ADAMTS2):c.3178+4A>G rs948167718
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.563A>G (p.Glu188Gly) rs772175576
NM_014244.5(ADAMTS2):c.655C>T (p.Pro219Ser) rs146217716
NM_014244.5(ADAMTS2):c.68T>C (p.Leu23Pro) rs565885690
NM_014244.5(ADAMTS2):c.710A>C (p.Asp237Ala) rs202197821
NM_014244.5(ADAMTS2):c.773G>A (p.Arg258His) rs1057524562
NM_014244.5(ADAMTS2):c.80_100dup (p.Leu27_Pro33dup) rs1064794627
NM_014244.5(ADAMTS2):c.80_88dup (p.Leu27_Pro29dup) rs775509290
NM_014244.5(ADAMTS2):c.847G>A (p.Gly283Arg) rs376856341
NM_014244.5(ADAMTS2):c.935A>G (p.Asn312Ser) rs528367185
NM_014244.5(ADAMTS2):c.991G>A (p.Glu331Lys) rs17667857

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