ClinVar Miner

List of variants in gene ADAMTS2 reported as benign

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Gene type:
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Total variants: 54
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HGVS dbSNP
GRCh37/hg19 5q35.3(chr5:178728830-178935665)x3
GRCh37/hg19 5q35.3(chr5:178730062-178935665)x4
GRCh38/hg38 5q35.3(chr5:179342470-179506406)x3
NM_014244.4(ADAMTS2):c.*1468A>G rs2059776
NM_014244.4(ADAMTS2):c.*1486C>A rs1863918
NM_014244.4(ADAMTS2):c.*1586A>G rs888760
NM_014244.4(ADAMTS2):c.*212A>C rs10479525
NM_014244.4(ADAMTS2):c.*2396C>T rs3797615
NM_014244.4(ADAMTS2):c.*2951G>A rs1044205
NM_014244.4(ADAMTS2):c.*2952T>A rs1044209
NM_014244.4(ADAMTS2):c.*842T>C rs10038484
NM_014244.4(ADAMTS2):c.1194C>T (p.Asp398=) rs2278221
NM_014244.4(ADAMTS2):c.1238+18G>A rs2278222
NM_014244.4(ADAMTS2):c.1281C>T (p.Asp427=) rs34424371
NM_014244.4(ADAMTS2):c.1308G>A (p.Ala436=) rs41285549
NM_014244.4(ADAMTS2):c.1458C>T (p.Tyr486=) rs61757478
NM_014244.4(ADAMTS2):c.1488C>T (p.Phe496=) rs147438064
NM_014244.4(ADAMTS2):c.1629+9G>A rs115550684
NM_014244.4(ADAMTS2):c.1630-18T>C rs2303638
NM_014244.4(ADAMTS2):c.1644A>G (p.Gly548=) rs61731454
NM_014244.4(ADAMTS2):c.1695C>T (p.Gly565=) rs116708837
NM_014244.4(ADAMTS2):c.1803G>A (p.Ser601=) rs76754323
NM_014244.4(ADAMTS2):c.1908C>T (p.His636=) rs1862211
NM_014244.4(ADAMTS2):c.1993G>A (p.Gly665Arg) rs35372714
NM_014244.4(ADAMTS2):c.2028C>T (p.Asp676=) rs1972715
NM_014244.4(ADAMTS2):c.2073C>T (p.Arg691=) rs149391669
NM_014244.4(ADAMTS2):c.220G>A (p.Val74Met) rs2271211
NM_014244.4(ADAMTS2):c.2291-8A>G rs140401199
NM_014244.4(ADAMTS2):c.2439C>T (p.His813=) rs141661592
NM_014244.4(ADAMTS2):c.2480G>A (p.Arg827Gln) rs35445112
NM_014244.4(ADAMTS2):c.2532C>T (p.Asp844=) rs2303644
NM_014244.4(ADAMTS2):c.2730A>G (p.Pro910=) rs6869261
NM_014244.4(ADAMTS2):c.2751-4G>A rs112155474
NM_014244.4(ADAMTS2):c.2959-16G>A rs6863024
NM_014244.4(ADAMTS2):c.2959-17C>T rs2303641
NM_014244.4(ADAMTS2):c.3014C>T (p.Ala1005Val) rs79330641
NM_014244.4(ADAMTS2):c.321T>C (p.Ser107=) rs2271212
NM_014244.4(ADAMTS2):c.3279T>C (p.Cys1093=) rs73806887
NM_014244.4(ADAMTS2):c.3480C>A (p.Ala1160=) rs34437036
NM_014244.4(ADAMTS2):c.3506G>T (p.Gly1169Val) rs117187367
NM_014244.4(ADAMTS2):c.3529C>T (p.Pro1177Ser) rs1054480
NM_014244.4(ADAMTS2):c.534+9G>C rs2271213
NM_014244.4(ADAMTS2):c.596C>T (p.Ala199Val) rs76704342
NM_014244.4(ADAMTS2):c.68T>C (p.Leu23Pro) rs565885690
NM_014244.4(ADAMTS2):c.68_70delTGC (p.Leu23del) rs568040559
NM_014244.4(ADAMTS2):c.68_70dupTGC (p.Leu23_Pro24insLeu) rs568040559
NM_014244.4(ADAMTS2):c.701A>G (p.Asp234Gly) rs59567206
NM_014244.4(ADAMTS2):c.722G>A (p.Arg241His) rs11750821
NM_014244.4(ADAMTS2):c.733G>A (p.Val245Ile) rs398829
NM_014244.4(ADAMTS2):c.764G>A (p.Arg255Gln) rs117222015
NM_014244.4(ADAMTS2):c.786G>A (p.Ala262=) rs423552
NM_014244.4(ADAMTS2):c.858C>T (p.His286=) rs66565583
NM_014244.4(ADAMTS2):c.936C>T (p.Asn312=) rs35462609
NM_021599.3(ADAMTS2):c.80_100dup (p.Pro33_Pro34insLeuLeuProProProProPro) rs1064794627

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