ClinVar Miner

List of variants in gene ADAMTS2 reported as likely benign for not specified

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Total variants: 64
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HGVS dbSNP
NM_014244.4(ADAMTS2):c.2210-21_2210-20delGT rs531944108
NM_014244.5(ADAMTS2):c.-38G>A rs1000819017
NM_014244.5(ADAMTS2):c.-7G>C rs1045542267
NM_014244.5(ADAMTS2):c.1083T>C (p.Asp361=) rs150079799
NM_014244.5(ADAMTS2):c.1122C>T (p.Ser374=) rs145109914
NM_014244.5(ADAMTS2):c.1164G>A (p.Pro388=) rs141348218
NM_014244.5(ADAMTS2):c.119_121CCG[5] (p.Ala43dup) rs1174228917
NM_014244.5(ADAMTS2):c.1239-12C>T rs772989447
NM_014244.5(ADAMTS2):c.1239-4G>A rs922294987
NM_014244.5(ADAMTS2):c.1308G>A (p.Ala436=) rs41285549
NM_014244.5(ADAMTS2):c.1382+12C>A rs773245710
NM_014244.5(ADAMTS2):c.1382+20C>A rs1057524448
NM_014244.5(ADAMTS2):c.1383-15G>A rs373540125
NM_014244.5(ADAMTS2):c.1383-16C>T rs377462612
NM_014244.5(ADAMTS2):c.140-7G>A rs759954552
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.1479C>G (p.Arg493=) rs901870480
NM_014244.5(ADAMTS2):c.1488C>T (p.Phe496=) rs147438064
NM_014244.5(ADAMTS2):c.1512G>A (p.Thr504=) rs141369064
NM_014244.5(ADAMTS2):c.1629+9G>A rs115550684
NM_014244.5(ADAMTS2):c.1641A>G (p.Lys547=) rs776592829
NM_014244.5(ADAMTS2):c.1644A>G (p.Gly548=) rs61731454
NM_014244.5(ADAMTS2):c.1695C>T (p.Gly565=) rs116708837
NM_014244.5(ADAMTS2):c.1902C>T (p.Phe634=) rs769205569
NM_014244.5(ADAMTS2):c.195C>T (p.Asp65=) rs1554099931
NM_014244.5(ADAMTS2):c.1993G>A (p.Gly665Arg) rs35372714
NM_014244.5(ADAMTS2):c.2073C>T (p.Arg691=) rs149391669
NM_014244.5(ADAMTS2):c.2085+11A>G rs139255728
NM_014244.5(ADAMTS2):c.2290+16G>A rs377081338
NM_014244.5(ADAMTS2):c.2376C>T (p.Gly792=) rs779908624
NM_014244.5(ADAMTS2):c.2458-19G>T rs1554124104
NM_014244.5(ADAMTS2):c.2617+13C>T rs756651045
NM_014244.5(ADAMTS2):c.2617+14G>A rs753127866
NM_014244.5(ADAMTS2):c.2617+19del rs753157368
NM_014244.5(ADAMTS2):c.2628C>T (p.Phe876=) rs371021469
NM_014244.5(ADAMTS2):c.2751-15G>A rs376602983
NM_014244.5(ADAMTS2):c.2751-4G>A rs112155474
NM_014244.5(ADAMTS2):c.2880T>C (p.Asn960=) rs1350390171
NM_014244.5(ADAMTS2):c.2892C>T (p.Pro964=) rs546361762
NM_014244.5(ADAMTS2):c.2958+20C>T rs200469634
NM_014244.5(ADAMTS2):c.2958+4C>T rs375345961
NM_014244.5(ADAMTS2):c.2970C>T (p.Thr990=) rs769689633
NM_014244.5(ADAMTS2):c.3014C>T (p.Ala1005Val) rs79330641
NM_014244.5(ADAMTS2):c.3018C>T (p.Asp1006=) rs150535792
NM_014244.5(ADAMTS2):c.3027C>T (p.Phe1009=) rs766033559
NM_014244.5(ADAMTS2):c.3279T>C (p.Cys1093=) rs73806887
NM_014244.5(ADAMTS2):c.3342C>T (p.Asn1114=) rs79606317
NM_014244.5(ADAMTS2):c.3607C>T (p.Arg1203Trp) rs144078893
NM_014244.5(ADAMTS2):c.3624C>T (p.Leu1208=) rs139420412
NM_014244.5(ADAMTS2):c.47_49TGC[10] (p.Leu22_Leu23dup) rs568040559
NM_014244.5(ADAMTS2):c.47_49TGC[11] (p.Leu21_Leu23dup) rs568040559
NM_014244.5(ADAMTS2):c.525C>T (p.Cys175=) rs140167371
NM_014244.5(ADAMTS2):c.596C>T (p.Ala199Val) rs76704342
NM_014244.5(ADAMTS2):c.689-18G>A rs202114393
NM_014244.5(ADAMTS2):c.689-19C>T rs201779376
NM_014244.5(ADAMTS2):c.68T>C (p.Leu23Pro) rs565885690
NM_014244.5(ADAMTS2):c.748G>A (p.Ala250Thr) rs143764421
NM_014244.5(ADAMTS2):c.759G>A (p.Ser253=) rs374180760
NM_014244.5(ADAMTS2):c.764G>A (p.Arg255Gln) rs117222015
NM_014244.5(ADAMTS2):c.789C>T (p.Asp263=) rs144235544
NM_014244.5(ADAMTS2):c.80_88dup (p.Leu27_Pro29dup) rs775509290
NM_014244.5(ADAMTS2):c.84_86GCC[7] (p.Pro34dup) rs770212030
NM_014244.5(ADAMTS2):c.867G>A (p.Lys289=) rs1191391499

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