ClinVar Miner

List of variants in gene DSG2 reported as uncertain significance for not provided

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Gene type:
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Total variants: 100
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HGVS dbSNP
NM_001943.5(DSG2):c.-11G>A rs727504450
NM_001943.5(DSG2):c.-21_6del (p.Met1_Ala2del)
NM_001943.5(DSG2):c.1003A>G (p.Thr335Ala) rs191564916
NM_001943.5(DSG2):c.1035GAA[1] (p.Lys346del) rs727502987
NM_001943.5(DSG2):c.1063G>A (p.Ala355Thr) rs201046640
NM_001943.5(DSG2):c.1072G>A (p.Ala358Thr) rs758537946
NM_001943.5(DSG2):c.1106A>T (p.Lys369Met)
NM_001943.5(DSG2):c.1130T>A (p.Val377Asp) rs794728085
NM_001943.5(DSG2):c.1173C>A (p.Ser391Arg) rs763242004
NM_001943.5(DSG2):c.1174G>A (p.Val392Ile) rs193922639
NM_001943.5(DSG2):c.1195G>A (p.Glu399Lys) rs774863785
NM_001943.5(DSG2):c.1281A>T (p.Arg427Ser) rs370547219
NM_001943.5(DSG2):c.1303G>A (p.Asp435Asn) rs370509593
NM_001943.5(DSG2):c.1346T>G (p.Leu449Arg) rs786205363
NM_001943.5(DSG2):c.1397C>T (p.Thr466Ile) rs769137357
NM_001943.5(DSG2):c.1460T>C (p.Ile487Thr) rs776525113
NM_001943.5(DSG2):c.1478A>G (p.Asn493Ser) rs375679311
NM_001943.5(DSG2):c.14C>T (p.Pro5Leu) rs530517936
NM_001943.5(DSG2):c.151T>C (p.Trp51Arg) rs1064794367
NM_001943.5(DSG2):c.1555G>T (p.Asp519Tyr) rs778119035
NM_001943.5(DSG2):c.1592T>G (p.Phe531Cys) rs200484060
NM_001943.5(DSG2):c.1605C>A (p.Asp535Glu) rs368718022
NM_001943.5(DSG2):c.1643G>A (p.Arg548His) rs551034751
NM_001943.5(DSG2):c.164C>T (p.Pro55Leu) rs748684045
NM_001943.5(DSG2):c.166G>A (p.Val56Met) rs121913013
NM_001943.5(DSG2):c.175C>T (p.Arg59Trp) rs749602291
NM_001943.5(DSG2):c.1795T>C (p.Cys599Arg) rs762413624
NM_001943.5(DSG2):c.1837G>A (p.Ala613Thr) rs368257724
NM_001943.5(DSG2):c.1843A>G (p.Ile615Val) rs794728087
NM_001943.5(DSG2):c.1885C>T (p.Pro629Ser) rs200804638
NM_001943.5(DSG2):c.1912G>A (p.Gly638Arg) rs201564919
NM_001943.5(DSG2):c.1959G>A (p.Met653Ile) rs794728088
NM_001943.5(DSG2):c.2065G>A (p.Gly689Ser)
NM_001943.5(DSG2):c.2074A>G (p.Lys692Glu) rs997161591
NM_001943.5(DSG2):c.2084C>T (p.Thr695Met) rs200137091
NM_001943.5(DSG2):c.208A>G (p.Ile70Val) rs769713919
NM_001943.5(DSG2):c.2155G>A (p.Glu719Lys) rs794728089
NM_001943.5(DSG2):c.216+3A>C rs774208829
NM_001943.5(DSG2):c.2165G>A (p.Arg722Lys) rs376819371
NM_001943.5(DSG2):c.2192A>C (p.Gln731Pro) rs202063433
NM_001943.5(DSG2):c.220C>A (p.His74Asn) rs772406363
NM_001943.5(DSG2):c.2234C>T (p.Thr745Met) rs727504783
NM_001943.5(DSG2):c.2242G>T (p.Ala748Ser) rs763994831
NM_001943.5(DSG2):c.2275G>A (p.Gly759Arg) rs765793636
NM_001943.5(DSG2):c.2360A>G (p.Asp787Gly) rs369868954
NM_001943.5(DSG2):c.2399C>G (p.Ser800Cys) rs794728090
NM_001943.5(DSG2):c.2434G>A (p.Gly812Ser) rs121913010
NM_001943.5(DSG2):c.2510C>A (p.Ala837Asp) rs756338201
NM_001943.5(DSG2):c.2548G>C (p.Glu850Gln) rs794728099
NM_001943.5(DSG2):c.2593A>C (p.Thr865Pro) rs866344768
NM_001943.5(DSG2):c.2646CTC[1] (p.Ser884del) rs794728095
NM_001943.5(DSG2):c.2690C>A (p.Ala897Asp) rs765238150
NM_001943.5(DSG2):c.2710C>G (p.Gln904Glu)
NM_001943.5(DSG2):c.2714A>C (p.Glu905Ala) rs1555628237
NM_001943.5(DSG2):c.2716A>G (p.Ile906Val) rs748894535
NM_001943.5(DSG2):c.2780C>T (p.Pro927Leu) rs146402368
NM_001943.5(DSG2):c.2800A>G (p.Ile934Val) rs1469730786
NM_001943.5(DSG2):c.2953G>A (p.Val985Ile) rs749540432
NM_001943.5(DSG2):c.3040G>A (p.Val1014Ile) rs200830807
NM_001943.5(DSG2):c.3044T>C (p.Met1015Thr) rs886053716
NM_001943.5(DSG2):c.3095C>T (p.Thr1032Ile)
NM_001943.5(DSG2):c.3144_3147del (p.Arg1049fs) rs758822081
NM_001943.5(DSG2):c.3167C>T (p.Thr1056Ile) rs767538450
NM_001943.5(DSG2):c.3233G>C (p.Gly1078Ala) rs1064795829
NM_001943.5(DSG2):c.3244C>G (p.Pro1082Ala) rs191300661
NM_001943.5(DSG2):c.3266G>T (p.Gly1089Val) rs200264407
NM_001943.5(DSG2):c.3281_3283delinsTTA (p.Gly1094_His1095delinsValAsn) rs386802145
NM_001943.5(DSG2):c.3293C>G (p.Ser1098Cys) rs2848673
NM_001943.5(DSG2):c.3318A>C (p.Arg1106Ser) rs1598827838
NM_001943.5(DSG2):c.3353C>T (p.Ser1118Phe) rs368703304
NM_001943.5(DSG2):c.424C>A (p.Pro142Thr) rs1005230453
NM_001943.5(DSG2):c.430G>A (p.Glu144Lys) rs199842209
NM_001943.5(DSG2):c.437G>T (p.Arg146Leu) rs113451409
NM_001943.5(DSG2):c.44T>A (p.Leu15Gln) rs372174546
NM_001943.5(DSG2):c.46A>G (p.Ile16Val) rs376660601
NM_001943.5(DSG2):c.470C>T (p.Pro157Leu) rs587782938
NM_001943.5(DSG2):c.545A>G (p.Asn182Ser) rs368512832
NM_001943.5(DSG2):c.562G>A (p.Glu188Lys) rs763948986
NM_001943.5(DSG2):c.613C>T (p.Pro205Ser) rs200946320
NM_001943.5(DSG2):c.650C>T (p.Thr217Ile) rs776720174
NM_001943.5(DSG2):c.653G>T (p.Gly218Val) rs794728082
NM_001943.5(DSG2):c.704A>G (p.Tyr235Cys) rs786205362
NM_001943.5(DSG2):c.716T>C (p.Val239Ala) rs200997703
NM_001943.5(DSG2):c.71T>C (p.Leu24Pro)
NM_001943.5(DSG2):c.770A>G (p.Gln257Arg) rs765118809
NM_001943.5(DSG2):c.841G>A (p.Val281Ile) rs201005720
NM_001943.5(DSG2):c.84C>G (p.Val28=) rs397516711
NM_001943.5(DSG2):c.862G>A (p.Val288Ile) rs780374242
NM_001943.5(DSG2):c.86T>C (p.Leu29Ser) rs786205361
NM_001943.5(DSG2):c.872C>T (p.Thr291Met) rs774563205
NM_001943.5(DSG2):c.874C>T (p.Arg292Cys) rs770921270
NM_001943.5(DSG2):c.875G>A (p.Arg292His) rs185821167
NM_001943.5(DSG2):c.880A>G (p.Lys294Glu) rs752432726
NM_001943.5(DSG2):c.889G>A (p.Asp297Asn) rs751012696
NM_001943.5(DSG2):c.928T>G (p.Phe310Val) rs1555671479
NM_001943.5(DSG2):c.955G>A (p.Gly319Ser) rs1064796086
NM_001943.5(DSG2):c.961T>A (p.Phe321Ile) rs201040643
NM_001943.5(DSG2):c.973A>G (p.Thr325Ala) rs745763739
NM_001943.5(DSG2):c.98A>G (p.Asn33Ser) rs727505205
NM_001943.5(DSG2):c.990C>G (p.Asn330Lys) rs140575919

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