ClinVar Miner

List of variants in gene DSG2 reported as likely benign for Cardiomyopathy

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Gene type:
ClinVar version:
Total variants: 188
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HGVS dbSNP
NM_001943.5(DSG2):c.1003A>G (p.Thr335Ala) rs191564916
NM_001943.5(DSG2):c.1015-14G>C
NM_001943.5(DSG2):c.1017A>G (p.Glu339=) rs1325947416
NM_001943.5(DSG2):c.1051A>G (p.Ser351Gly) rs139326669
NM_001943.5(DSG2):c.1062C>T (p.Val354=) rs369233023
NM_001943.5(DSG2):c.1063G>A (p.Ala355Thr) rs201046640
NM_001943.5(DSG2):c.1089G>A (p.Ser363=) rs372598337
NM_001943.5(DSG2):c.1110T>C (p.Pro370=) rs772805008
NM_001943.5(DSG2):c.1116C>G (p.Pro372=) rs542079618
NM_001943.5(DSG2):c.1119T>C (p.Ile373=) rs770547012
NM_001943.5(DSG2):c.1173C>T (p.Ser391=) rs763242004
NM_001943.5(DSG2):c.1188T>C (p.Tyr396=)
NM_001943.5(DSG2):c.1194C>T (p.Ser398=)
NM_001943.5(DSG2):c.121C>A (p.His41Asn) rs201499704
NM_001943.5(DSG2):c.1266A>G (p.Leu422=) rs770359142
NM_001943.5(DSG2):c.1274A>G (p.His425Arg)
NM_001943.5(DSG2):c.1278A>G (p.Ala426=)
NM_001943.5(DSG2):c.1284T>C (p.Tyr428=) rs202095254
NM_001943.5(DSG2):c.1299T>C (p.Asp433=) rs367548984
NM_001943.5(DSG2):c.1392A>G (p.Thr464=) rs373918593
NM_001943.5(DSG2):c.1458T>C (p.Leu486=)
NM_001943.5(DSG2):c.1476C>T (p.Ile492=)
NM_001943.5(DSG2):c.147C>T (p.Arg49=) rs531036279
NM_001943.5(DSG2):c.1491C>T (p.Pro497=) rs587780928
NM_001943.5(DSG2):c.1503G>T (p.Glu501Asp) rs1191142951
NM_001943.5(DSG2):c.1515A>T (p.Thr505=)
NM_001943.5(DSG2):c.1524C>T (p.His508=)
NM_001943.5(DSG2):c.1533G>A (p.Glu511=)
NM_001943.5(DSG2):c.1536T>C (p.Tyr512=)
NM_001943.5(DSG2):c.1548T>C (p.Thr516=)
NM_001943.5(DSG2):c.1596C>T (p.Ser532=)
NM_001943.5(DSG2):c.15G>C (p.Pro5=) rs772663614
NM_001943.5(DSG2):c.1640C>T (p.Ala547Val)
NM_001943.5(DSG2):c.1643G>A (p.Arg548His) rs551034751
NM_001943.5(DSG2):c.1652-13C>T
NM_001943.5(DSG2):c.1652-5T>C
NM_001943.5(DSG2):c.1652-8C>T rs770497608
NM_001943.5(DSG2):c.165C>T (p.Pro55=) rs780650457
NM_001943.5(DSG2):c.166G>A (p.Val56Met) rs121913013
NM_001943.5(DSG2):c.1688T>G (p.Leu563Arg) rs780469370
NM_001943.5(DSG2):c.1707G>C (p.Gln569His)
NM_001943.5(DSG2):c.177G>C (p.Arg59=) rs1568104857
NM_001943.5(DSG2):c.1836C>T (p.Pro612=)
NM_001943.5(DSG2):c.1845T>C (p.Ile615=)
NM_001943.5(DSG2):c.1847C>T (p.Ala616Val) rs375527314
NM_001943.5(DSG2):c.1848G>A (p.Ala616=)
NM_001943.5(DSG2):c.1848G>C (p.Ala616=)
NM_001943.5(DSG2):c.1851C>T (p.Leu617=) rs202057770
NM_001943.5(DSG2):c.1866T>C (p.Phe622=)
NM_001943.5(DSG2):c.1867C>T (p.Leu623=) rs1456806722
NM_001943.5(DSG2):c.1878A>G (p.Leu626=) rs771576658
NM_001943.5(DSG2):c.1920C>T (p.Gly640=) rs775642244
NM_001943.5(DSG2):c.1947C>T (p.Gly649=)
NM_001943.5(DSG2):c.1960C>T (p.Leu654=)
NM_001943.5(DSG2):c.2001+3C>G rs746471051
NM_001943.5(DSG2):c.2004G>A (p.Val668=) rs773645222
NM_001943.5(DSG2):c.2043A>T (p.Leu681=)
NM_001943.5(DSG2):c.2085G>A (p.Thr695=) rs554396523
NM_001943.5(DSG2):c.2115C>G (p.Val705=)
NM_001943.5(DSG2):c.216+8del
NM_001943.5(DSG2):c.2169C>T (p.Ser723=)
NM_001943.5(DSG2):c.2172G>A (p.Leu724=)
NM_001943.5(DSG2):c.2178T>C (p.Ser726=)
NM_001943.5(DSG2):c.2203G>A (p.Ala735Thr)
NM_001943.5(DSG2):c.2214T>G (p.Ala738=)
NM_001943.5(DSG2):c.221A>G (p.His74Arg) rs201855245
NM_001943.5(DSG2):c.2220G>C (p.Met740Ile)
NM_001943.5(DSG2):c.2224A>G (p.Thr742Ala)
NM_001943.5(DSG2):c.222T>C (p.His74=) rs367797047
NM_001943.5(DSG2):c.2234C>T (p.Thr745Met) rs727504783
NM_001943.5(DSG2):c.2235G>A (p.Thr745=) rs759572082
NM_001943.5(DSG2):c.2241C>T (p.Thr747=) rs767628208
NM_001943.5(DSG2):c.2304C>T (p.Asn768=)
NM_001943.5(DSG2):c.2335-12_2335-8dup
NM_001943.5(DSG2):c.2335-7A>C
NM_001943.5(DSG2):c.2335-8C>G
NM_001943.5(DSG2):c.2339C>T (p.Ala780Val) rs547406532
NM_001943.5(DSG2):c.2340G>A (p.Ala780=)
NM_001943.5(DSG2):c.2340G>T (p.Ala780=) rs375539435
NM_001943.5(DSG2):c.2360A>G (p.Asp787Gly) rs369868954
NM_001943.5(DSG2):c.2366A>G (p.Asn789Ser)
NM_001943.5(DSG2):c.2368C>T (p.His790Tyr) rs114544564
NM_001943.5(DSG2):c.2373A>G (p.Thr791=)
NM_001943.5(DSG2):c.2397T>C (p.Tyr799=)
NM_001943.5(DSG2):c.2418G>A (p.Ser806=)
NM_001943.5(DSG2):c.2421G>T (p.Leu807=) rs374775982
NM_001943.5(DSG2):c.2439T>C (p.Cys813=)
NM_001943.5(DSG2):c.2442C>T (p.Cys814=)
NM_001943.5(DSG2):c.2470C>T (p.Arg824Cys) rs201845396
NM_001943.5(DSG2):c.2472C>T (p.Arg824=)
NM_001943.5(DSG2):c.2491C>T (p.Leu831Phe)
NM_001943.5(DSG2):c.2563C>A (p.Gln855Lys)
NM_001943.5(DSG2):c.2583A>G (p.Thr861=) rs774775322
NM_001943.5(DSG2):c.2597C>T (p.Ala866Val)
NM_001943.5(DSG2):c.2619A>G (p.Gln873=)
NM_001943.5(DSG2):c.2628T>C (p.Val876=) rs775842543
NM_001943.5(DSG2):c.2643C>T (p.Thr881=) rs180695545
NM_001943.5(DSG2):c.2712G>A (p.Gln904=)
NM_001943.5(DSG2):c.2721C>T (p.Val907=)
NM_001943.5(DSG2):c.273A>G (p.Gly91=) rs376944801
NM_001943.5(DSG2):c.2742T>C (p.Ser914=) rs529198523
NM_001943.5(DSG2):c.2750C>T (p.Ala917Val) rs775670183
NM_001943.5(DSG2):c.2751G>A (p.Ala917=) rs763063602
NM_001943.5(DSG2):c.2766A>G (p.Thr922=)
NM_001943.5(DSG2):c.2780C>T (p.Pro927Leu) rs146402368
NM_001943.5(DSG2):c.2826A>G (p.Thr942=)
NM_001943.5(DSG2):c.2833A>G (p.Thr945Ala)
NM_001943.5(DSG2):c.2853G>A (p.Val951=) rs775759794
NM_001943.5(DSG2):c.2898G>A (p.Arg966=) rs746543384
NM_001943.5(DSG2):c.2906C>T (p.Ala969Val) rs373598034
NM_001943.5(DSG2):c.2913T>G (p.Ala971=) rs200793530
NM_001943.5(DSG2):c.2917A>G (p.Thr973Ala)
NM_001943.5(DSG2):c.2959G>T (p.Val987Phe) rs141405267
NM_001943.5(DSG2):c.297T>C (p.Phe99=)
NM_001943.5(DSG2):c.2982T>C (p.Pro994=)
NM_001943.5(DSG2):c.2991T>A (p.Gly997=) rs765129273
NM_001943.5(DSG2):c.2997G>A (p.Ser999=) rs763888499
NM_001943.5(DSG2):c.3039C>T (p.Tyr1013=)
NM_001943.5(DSG2):c.3075C>T (p.Pro1025=)
NM_001943.5(DSG2):c.3082G>A (p.Gly1028Ser) rs150864240
NM_001943.5(DSG2):c.3095C>T (p.Thr1032Ile)
NM_001943.5(DSG2):c.3096T>G (p.Thr1032=)
NM_001943.5(DSG2):c.30C>A (p.Ala10=) rs1568098547
NM_001943.5(DSG2):c.3112A>G (p.Ile1038Val) rs774113529
NM_001943.5(DSG2):c.3118G>A (p.Val1040Ile) rs201966605
NM_001943.5(DSG2):c.3147A>G (p.Arg1049=) rs973445903
NM_001943.5(DSG2):c.3175T>A (p.Ser1059Thr) rs201786158
NM_001943.5(DSG2):c.3195T>C (p.Thr1065=) rs544981484
NM_001943.5(DSG2):c.31C>T (p.Leu11=) rs1220091298
NM_001943.5(DSG2):c.3204T>G (p.Ser1068=)
NM_001943.5(DSG2):c.3205A>G (p.Met1069Val)
NM_001943.5(DSG2):c.3210G>T (p.Thr1070=)
NM_001943.5(DSG2):c.3216G>A (p.Arg1072=)
NM_001943.5(DSG2):c.3224C>T (p.Thr1075Met)
NM_001943.5(DSG2):c.3225G>A (p.Thr1075=) rs773954315
NM_001943.5(DSG2):c.3228G>A (p.Val1076=) rs373966845
NM_001943.5(DSG2):c.3243C>T (p.Val1081=) rs11542379
NM_001943.5(DSG2):c.3244C>G (p.Pro1082Ala) rs191300661
NM_001943.5(DSG2):c.3266G>A (p.Gly1089Asp) rs200264407
NM_001943.5(DSG2):c.3291T>C (p.Asn1097=) rs757473850
NM_001943.5(DSG2):c.3295A>G (p.Thr1099Ala) rs79068489
NM_001943.5(DSG2):c.3306A>G (p.Thr1102=)
NM_001943.5(DSG2):c.3309T>C (p.Ser1103=) rs1195224927
NM_001943.5(DSG2):c.379-3C>T rs376556524
NM_001943.5(DSG2):c.390C>T (p.Tyr130=) rs369489095
NM_001943.5(DSG2):c.435A>G (p.Leu145=)
NM_001943.5(DSG2):c.437G>T (p.Arg146Leu) rs113451409
NM_001943.5(DSG2):c.447T>C (p.Val149=)
NM_001943.5(DSG2):c.44T>A (p.Leu15Gln) rs372174546
NM_001943.5(DSG2):c.45+6T>C
NM_001943.5(DSG2):c.46-3C>T rs777302616
NM_001943.5(DSG2):c.465C>T (p.Asn155=) rs751814575
NM_001943.5(DSG2):c.511T>C (p.Leu171=)
NM_001943.5(DSG2):c.545A>G (p.Asn182Ser) rs368512832
NM_001943.5(DSG2):c.564G>A (p.Glu188=)
NM_001943.5(DSG2):c.57C>T (p.Asn19=) rs587780925
NM_001943.5(DSG2):c.582G>A (p.Ser194=)
NM_001943.5(DSG2):c.618T>A (p.Ala206=) rs397516710
NM_001943.5(DSG2):c.624T>G (p.Pro208=) rs1275487240
NM_001943.5(DSG2):c.648T>C (p.Asp216=)
NM_001943.5(DSG2):c.684C>T (p.Asp228=) rs1568105759
NM_001943.5(DSG2):c.691-9G>A
NM_001943.5(DSG2):c.693A>G (p.Glu231=)
NM_001943.5(DSG2):c.6G>T (p.Ala2=)
NM_001943.5(DSG2):c.706A>G (p.Thr236Ala) rs727502985
NM_001943.5(DSG2):c.713C>T (p.Thr238Ile)
NM_001943.5(DSG2):c.716T>C (p.Val239Ala) rs200997703
NM_001943.5(DSG2):c.720A>G (p.Glu240=)
NM_001943.5(DSG2):c.783T>A (p.Arg261=) rs369869320
NM_001943.5(DSG2):c.78A>G (p.Leu26=)
NM_001943.5(DSG2):c.795C>G (p.Val265=) rs771324254
NM_001943.5(DSG2):c.798T>C (p.Asn266=)
NM_001943.5(DSG2):c.813A>G (p.Val271=)
NM_001943.5(DSG2):c.82-3T>C
NM_001943.5(DSG2):c.82-4A>G
NM_001943.5(DSG2):c.828+5C>T
NM_001943.5(DSG2):c.829-11A>G
NM_001943.5(DSG2):c.829-4G>A rs376424003
NM_001943.5(DSG2):c.829-9G>C
NM_001943.5(DSG2):c.834A>G (p.Glu278=)
NM_001943.5(DSG2):c.84C>G (p.Val28=) rs397516711
NM_001943.5(DSG2):c.852T>C (p.Asn284=) rs62095193
NM_001943.5(DSG2):c.872C>T (p.Thr291Met) rs774563205
NM_001943.5(DSG2):c.873G>A (p.Thr291=) rs760706353
NM_001943.5(DSG2):c.891T>C (p.Asp297=)
NM_001943.5(DSG2):c.938C>T (p.Ala313Val)
NM_001943.5(DSG2):c.990C>T (p.Asn330=) rs140575919
NM_001943.5(DSG2):c.996A>G (p.Gly332=)

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