ClinVar Miner

List of variants in gene DSG2 reported as likely benign for not provided

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Gene type:
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Total variants: 49
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HGVS dbSNP
NM_001943.5(DSG2):c.1017A>G (p.Glu339=) rs1325947416
NM_001943.5(DSG2):c.1047C>T (p.Asp349=) rs1598816361
NM_001943.5(DSG2):c.1089G>A (p.Ser363=) rs372598337
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.1280+4AG[3] rs876657791
NM_001943.5(DSG2):c.1280+8A>G rs377662063
NM_001943.5(DSG2):c.1281-16G>T rs756914573
NM_001943.5(DSG2):c.1303G>A (p.Asp435Asn) rs370509593
NM_001943.5(DSG2):c.1317T>C (p.Ser439=) rs727505064
NM_001943.5(DSG2):c.1376A>G (p.Tyr459Cys) rs576404380
NM_001943.5(DSG2):c.1479C>T (p.Asn493=) rs778100657
NM_001943.5(DSG2):c.1524C>T (p.His508=)
NM_001943.5(DSG2):c.159C>T (p.Thr53=) rs959566645
NM_001943.5(DSG2):c.1688T>G (p.Leu563Arg) rs780469370
NM_001943.5(DSG2):c.1781T>C (p.Leu594Pro) rs199681901
NM_001943.5(DSG2):c.1847C>T (p.Ala616Val) rs375527314
NM_001943.5(DSG2):c.1986A>G (p.Ala662=) rs1598823030
NM_001943.5(DSG2):c.2010A>G (p.Pro670=) rs777621113
NM_001943.5(DSG2):c.2085G>C (p.Thr695=) rs554396523
NM_001943.5(DSG2):c.2127T>C (p.His709=) rs876657457
NM_001943.5(DSG2):c.2234C>T (p.Thr745Met) rs727504783
NM_001943.5(DSG2):c.2335-9T>C rs757355636
NM_001943.5(DSG2):c.2339C>T (p.Ala780Val) rs547406532
NM_001943.5(DSG2):c.2340G>T (p.Ala780=) rs375539435
NM_001943.5(DSG2):c.2368C>T (p.His790Tyr) rs114544564
NM_001943.5(DSG2):c.273A>G (p.Gly91=) rs376944801
NM_001943.5(DSG2):c.2766A>C (p.Thr922=) rs1347885484
NM_001943.5(DSG2):c.3171G>A (p.Leu1057=) rs376020729
NM_001943.5(DSG2):c.31C>T (p.Leu11=) rs1220091298
NM_001943.5(DSG2):c.3209C>T (p.Thr1070Met) rs149617776
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.3295A>G (p.Thr1099Ala) rs79068489
NM_001943.5(DSG2):c.3309T>C (p.Ser1103=) rs1195224927
NM_001943.5(DSG2):c.3354C>G (p.Ser1118=) rs879254344
NM_001943.5(DSG2):c.379-22_379-18del rs1598810622
NM_001943.5(DSG2):c.379-4T>C rs753141182
NM_001943.5(DSG2):c.437G>T (p.Arg146Leu) rs113451409
NM_001943.5(DSG2):c.45+10G>A rs776975980
NM_001943.5(DSG2):c.600C>A (p.Ile200=) rs535646295
NM_001943.5(DSG2):c.624T>G (p.Pro208=) rs1275487240
NM_001943.5(DSG2):c.81+7A>G rs763204534
NM_001943.5(DSG2):c.852T>C (p.Asn284=) rs62095193
NM_001943.5(DSG2):c.873G>A (p.Thr291=) rs760706353
NM_001943.5(DSG2):c.888C>T (p.Phe296=) rs975297970
NM_001943.5(DSG2):c.990C>T (p.Asn330=) rs140575919
NM_001943.5(DSG2):c.99T>C (p.Asn33=) rs1598809953

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