ClinVar Miner

List of variants in gene DSG2 reported as likely benign for Cardiovascular phenotype

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Gene type:
ClinVar version:
Total variants: 159
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HGVS dbSNP gnomAD frequency
NM_001943.5(DSG2):c.1051A>G (p.Ser351Gly) rs139326669 0.00246
NM_001943.5(DSG2):c.3082G>A (p.Gly1028Ser) rs150864240 0.00196
NM_001943.5(DSG2):c.1174G>A (p.Val392Ile) rs193922639 0.00158
NM_001943.5(DSG2):c.166G>A (p.Val56Met) rs121913013 0.00150
NM_001943.5(DSG2):c.3295A>G (p.Thr1099Ala) rs79068489 0.00137
NM_001943.5(DSG2):c.2368C>T (p.His790Tyr) rs114544564 0.00130
NM_001943.5(DSG2):c.2703A>G (p.Lys901=) rs113591687 0.00114
NM_001943.5(DSG2):c.221A>G (p.His74Arg) rs201855245 0.00104
NM_001943.5(DSG2):c.852T>C (p.Asn284=) rs62095193 0.00061
NM_001943.5(DSG2):c.1003A>G (p.Thr335Ala) rs191564916 0.00060
NM_001943.5(DSG2):c.*2C>T rs183494886 0.00054
NM_001943.5(DSG2):c.437G>T (p.Arg146Leu) rs113451409 0.00054
NM_001943.5(DSG2):c.121C>A (p.His41Asn) rs201499704 0.00039
NM_001943.5(DSG2):c.1781T>C (p.Leu594Pro) rs199681901 0.00038
NM_001943.5(DSG2):c.3266G>A (p.Gly1089Asp) rs200264407 0.00038
NM_001943.5(DSG2):c.716T>C (p.Val239Ala) rs200997703 0.00037
NM_001943.5(DSG2):c.2192A>C (p.Gln731Pro) rs202063433 0.00032
NM_001943.5(DSG2):c.2913T>G (p.Ala971=) rs200793530 0.00024
NM_001943.5(DSG2):c.1851C>T (p.Leu617=) rs202057770 0.00017
NM_001943.5(DSG2):c.1912G>A (p.Gly638Arg) rs201564919 0.00016
NM_001943.5(DSG2):c.783T>A (p.Arg261=) rs369869320 0.00016
NM_001943.5(DSG2):c.2305G>A (p.Glu769Lys) rs371146201 0.00015
NM_001943.5(DSG2):c.3353C>T (p.Ser1118Phe) rs368703304 0.00014
NM_001943.5(DSG2):c.148G>A (p.Ala50Thr) rs1267795586 0.00013
NM_001943.5(DSG2):c.2744G>C (p.Arg915Thr) rs375358300 0.00013
NM_001943.5(DSG2):c.545A>G (p.Asn182Ser) rs368512832 0.00013
NM_001943.5(DSG2):c.3283C>A (p.His1095Asn) rs140193292 0.00012
NM_001943.5(DSG2):c.1299T>C (p.Asp433=) rs367548984 0.00011
NM_001943.5(DSG2):c.1478A>G (p.Asn493Ser) rs375679311 0.00011
NM_001943.5(DSG2):c.2360A>G (p.Asp787Gly) rs369868954 0.00011
NM_001943.5(DSG2):c.2506C>G (p.Leu836Val) rs767979763 0.00011
NM_001943.5(DSG2):c.1597G>A (p.Val533Ile) rs199761749 0.00010
NM_001943.5(DSG2):c.2643C>T (p.Thr881=) rs180695545 0.00010
NM_001943.5(DSG2):c.147C>T (p.Arg49=) rs531036279 0.00009
NM_001943.5(DSG2):c.2096G>T (p.Ser699Ile) rs727504770 0.00009
NM_001943.5(DSG2):c.3195T>C (p.Thr1065=) rs544981484 0.00007
NM_001943.5(DSG2):c.3244C>G (p.Pro1082Ala) rs191300661 0.00007
NM_001943.5(DSG2):c.600C>A (p.Ile200=) rs535646295 0.00007
NM_001943.5(DSG2):c.1089G>A (p.Ser363=) rs372598337 0.00006
NM_001943.5(DSG2):c.1491C>T (p.Pro497=) rs587780928 0.00006
NM_001943.5(DSG2):c.1643G>A (p.Arg548His) rs551034751 0.00006
NM_001943.5(DSG2):c.2085G>A (p.Thr695=) rs554396523 0.00006
NM_001943.5(DSG2):c.2241C>T (p.Thr747=) rs767628208 0.00006
NM_001943.5(DSG2):c.513G>T (p.Leu171Phe) rs199926617 0.00006
NM_001943.5(DSG2):c.165C>T (p.Pro55=) rs780650457 0.00005
NM_001943.5(DSG2):c.2471G>A (p.Arg824His) rs376858770 0.00005
NM_001943.5(DSG2):c.2780C>T (p.Pro927Leu) rs146402368 0.00005
NM_001943.5(DSG2):c.1063G>A (p.Ala355Thr) rs201046640 0.00004
NM_001943.5(DSG2):c.1110T>C (p.Pro370=) rs772805008 0.00004
NM_001943.5(DSG2):c.1920C>T (p.Gly640=) rs775642244 0.00004
NM_001943.5(DSG2):c.2004G>A (p.Val668=) rs773645222 0.00004
NM_001943.5(DSG2):c.2470C>T (p.Arg824Cys) rs201845396 0.00004
NM_001943.5(DSG2):c.273A>G (p.Gly91=) rs376944801 0.00004
NM_001943.5(DSG2):c.2906C>T (p.Ala969Val) rs373598034 0.00004
NM_001943.5(DSG2):c.2959G>T (p.Val987Phe) rs141405267 0.00004
NM_001943.5(DSG2):c.3118G>A (p.Val1040Ile) rs201966605 0.00004
NM_001943.5(DSG2):c.3171G>A (p.Leu1057=) rs376020729 0.00004
NM_001943.5(DSG2):c.390C>T (p.Tyr130=) rs369489095 0.00004
NM_001943.5(DSG2):c.873G>A (p.Thr291=) rs760706353 0.00004
NM_001943.5(DSG2):c.1119T>C (p.Ile373=) rs770547012 0.00003
NM_001943.5(DSG2):c.1481A>C (p.Asp494Ala) rs193298428 0.00003
NM_001943.5(DSG2):c.1524C>T (p.His508=) rs560004953 0.00003
NM_001943.5(DSG2):c.1536T>C (p.Tyr512=) rs952187023 0.00003
NM_001943.5(DSG2):c.2162A>G (p.His721Arg) rs756912703 0.00003
NM_001943.5(DSG2):c.2304C>T (p.Asn768=) rs368514815 0.00003
NM_001943.5(DSG2):c.2340G>T (p.Ala780=) rs375539435 0.00003
NM_001943.5(DSG2):c.2421G>T (p.Leu807=) rs374775982 0.00003
NM_001943.5(DSG2):c.2638A>C (p.Asn880His) rs745617885 0.00003
NM_001943.5(DSG2):c.3210G>A (p.Thr1070=) rs771104963 0.00003
NM_001943.5(DSG2):c.55A>G (p.Asn19Asp) rs185266383 0.00003
NM_001943.5(DSG2):c.706A>G (p.Thr236Ala) rs727502985 0.00003
NM_001943.5(DSG2):c.84C>G (p.Val28=) rs397516711 0.00003
NM_001943.5(DSG2):c.2100C>T (p.Ser700=) rs397516704 0.00002
NM_001943.5(DSG2):c.2339C>T (p.Ala780Val) rs547406532 0.00002
NM_001943.5(DSG2):c.2853G>A (p.Val951=) rs775759794 0.00002
NM_001943.5(DSG2):c.2997G>A (p.Ser999=) rs763888499 0.00002
NM_001943.5(DSG2):c.3225G>A (p.Thr1075=) rs773954315 0.00002
NM_001943.5(DSG2):c.3291T>C (p.Asn1097=) rs757473850 0.00002
NM_001943.5(DSG2):c.57C>T (p.Asn19=) rs587780925 0.00002
NM_001943.5(DSG2):c.675T>C (p.Val225=) rs576938518 0.00002
NM_001943.5(DSG2):c.86T>C (p.Leu29Ser) rs786205361 0.00002
NM_001943.5(DSG2):c.1017A>G (p.Glu339=) rs1325947416 0.00001
NM_001943.5(DSG2):c.1116C>G (p.Pro372=) rs542079618 0.00001
NM_001943.5(DSG2):c.1173C>T (p.Ser391=) rs763242004 0.00001
NM_001943.5(DSG2):c.1209A>G (p.Arg403=) rs1467727719 0.00001
NM_001943.5(DSG2):c.1251T>C (p.Asp417=) rs942476545 0.00001
NM_001943.5(DSG2):c.1284T>C (p.Tyr428=) rs202095254 0.00001
NM_001943.5(DSG2):c.1292T>C (p.Leu431Ser) rs540113579 0.00001
NM_001943.5(DSG2):c.1434A>G (p.Arg478=) rs755732646 0.00001
NM_001943.5(DSG2):c.1525G>A (p.Asp509Asn) rs753406968 0.00001
NM_001943.5(DSG2):c.1596C>T (p.Ser532=) rs775653162 0.00001
NM_001943.5(DSG2):c.159C>T (p.Thr53=) rs959566645 0.00001
NM_001943.5(DSG2):c.1624G>C (p.Glu542Gln) rs376784940 0.00001
NM_001943.5(DSG2):c.1821T>C (p.Tyr607=) rs1230368091 0.00001
NM_001943.5(DSG2):c.1836C>T (p.Pro612=) rs374288967 0.00001
NM_001943.5(DSG2):c.2010A>G (p.Pro670=) rs777621113 0.00001
NM_001943.5(DSG2):c.2136C>T (p.Ser712=) rs762885119 0.00001
NM_001943.5(DSG2):c.2397T>C (p.Tyr799=) rs200201181 0.00001
NM_001943.5(DSG2):c.2418G>A (p.Ser806=) rs751831001 0.00001
NM_001943.5(DSG2):c.2538T>C (p.Asp846=) rs755061815 0.00001
NM_001943.5(DSG2):c.2583A>G (p.Thr861=) rs774775322 0.00001
NM_001943.5(DSG2):c.2628T>C (p.Val876=) rs775842543 0.00001
NM_001943.5(DSG2):c.269C>T (p.Thr90Ile) rs772744115 0.00001
NM_001943.5(DSG2):c.2742T>C (p.Ser914=) rs529198523 0.00001
NM_001943.5(DSG2):c.2751G>A (p.Ala917=) rs763063602 0.00001
NM_001943.5(DSG2):c.297T>C (p.Phe99=) rs1045965107 0.00001
NM_001943.5(DSG2):c.3224C>T (p.Thr1075Met) rs943749481 0.00001
NM_001943.5(DSG2):c.447T>C (p.Val149=) rs1389484271 0.00001
NM_001943.5(DSG2):c.465C>T (p.Asn155=) rs751814575 0.00001
NM_001943.5(DSG2):c.561T>C (p.Asp187=) rs573318445 0.00001
NM_001943.5(DSG2):c.582G>A (p.Ser194=) rs748768578 0.00001
NM_001943.5(DSG2):c.648T>C (p.Asp216=) rs1235715453 0.00001
NM_001943.5(DSG2):c.693A>G (p.Glu231=) rs775582591 0.00001
NM_001943.5(DSG2):c.789G>A (p.Leu263=) rs1389678806 0.00001
NM_001943.5(DSG2):c.795C>G (p.Val265=) rs771324254 0.00001
NM_001943.5(DSG2):c.1062C>T (p.Val354=) rs369233023
NM_001943.5(DSG2):c.1377T>C (p.Tyr459=)
NM_001943.5(DSG2):c.138G>T (p.Arg46=) rs2073117347
NM_001943.5(DSG2):c.1578T>C (p.Ser526=)
NM_001943.5(DSG2):c.1593C>T (p.Phe531=)
NM_001943.5(DSG2):c.1710C>T (p.Phe570=)
NM_001943.5(DSG2):c.1724A>G (p.Asn575Ser) rs727502988
NM_001943.5(DSG2):c.1743T>C (p.Pro581=)
NM_001943.5(DSG2):c.1848G>A (p.Ala616=) rs372349945
NM_001943.5(DSG2):c.1848G>T (p.Ala616=) rs372349945
NM_001943.5(DSG2):c.1938C>T (p.Pro646=)
NM_001943.5(DSG2):c.2085G>C (p.Thr695=) rs554396523
NM_001943.5(DSG2):c.2235G>A (p.Thr745=) rs759572082
NM_001943.5(DSG2):c.2242G>A (p.Ala748Thr) rs763994831
NM_001943.5(DSG2):c.2340G>A (p.Ala780=) rs375539435
NM_001943.5(DSG2):c.2343C>T (p.Ala781=)
NM_001943.5(DSG2):c.2376C>G (p.Ala792=)
NM_001943.5(DSG2):c.2385C>T (p.Cys795=)
NM_001943.5(DSG2):c.2415A>G (p.Glu805=)
NM_001943.5(DSG2):c.2511T>G (p.Ala837=)
NM_001943.5(DSG2):c.2562A>G (p.Arg854=)
NM_001943.5(DSG2):c.261C>T (p.Tyr87=)
NM_001943.5(DSG2):c.2676A>G (p.Lys892=)
NM_001943.5(DSG2):c.2691C>A (p.Ala897=)
NM_001943.5(DSG2):c.2814T>C (p.Thr938=)
NM_001943.5(DSG2):c.2847C>A (p.Thr949=)
NM_001943.5(DSG2):c.2856C>T (p.Ile952=)
NM_001943.5(DSG2):c.3030T>C (p.Asp1010=)
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.3210G>T (p.Thr1070=) rs771104963
NM_001943.5(DSG2):c.3281G>T (p.Gly1094Val)
NM_001943.5(DSG2):c.3281_3283delinsTTA (p.Gly1094_His1095delinsValAsn) rs386802145
NM_001943.5(DSG2):c.3306A>G (p.Thr1102=) rs747930194
NM_001943.5(DSG2):c.3306A>T (p.Thr1102=)
NM_001943.5(DSG2):c.3333C>T (p.Ser1111=)
NM_001943.5(DSG2):c.369A>G (p.Pro123=) rs2144315797
NM_001943.5(DSG2):c.468A>G (p.Glu156=)
NM_001943.5(DSG2):c.762A>G (p.Lys254=)
NM_001943.5(DSG2):c.81+16G>T
NM_001943.5(DSG2):c.82-4A>G rs1332379061
NM_001943.5(DSG2):c.846A>G (p.Glu282=) rs752126487
NM_001943.5(DSG2):c.885G>A (p.Val295=) rs534674777
NM_001943.5(DSG2):c.888C>T (p.Phe296=) rs975297970

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