ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 98
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HGVS dbSNP
NM_001943.5(DSG2):c.*2C>T rs183494886
NM_001943.5(DSG2):c.-16C>G rs1057523171
NM_001943.5(DSG2):c.-1G>C rs1012160082
NM_001943.5(DSG2):c.-22G>A rs955882030
NM_001943.5(DSG2):c.1003A>G (p.Thr335Ala) rs191564916
NM_001943.5(DSG2):c.1051A>G (p.Ser351Gly) rs139326669
NM_001943.5(DSG2):c.1110T>C (p.Pro370=) rs772805008
NM_001943.5(DSG2):c.1174G>A (p.Val392Ile) rs193922639
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.1280+18G>C rs141175168
NM_001943.5(DSG2):c.1280+4AG[3] rs876657791
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.1303G>A (p.Asp435Asn) rs370509593
NM_001943.5(DSG2):c.1317T>C (p.Ser439=) rs727505064
NM_001943.5(DSG2):c.1392A>G (p.Thr464=) rs373918593
NM_001943.5(DSG2):c.1410G>A (p.Val470=) rs1036402724
NM_001943.5(DSG2):c.1463A>G (p.Asn488Ser) rs794728078
NM_001943.5(DSG2):c.1479C>T (p.Asn493=) rs778100657
NM_001943.5(DSG2):c.147C>T (p.Arg49=) rs531036279
NM_001943.5(DSG2):c.1550C>T (p.Ala517Val) rs200509948
NM_001943.5(DSG2):c.1573A>G (p.Asn525Asp) rs794728079
NM_001943.5(DSG2):c.1597G>A (p.Val533Ile) rs199761749
NM_001943.5(DSG2):c.1643G>A (p.Arg548His) rs551034751
NM_001943.5(DSG2):c.1652-12C>T rs140850369
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.1724A>G (p.Asn575Ser) rs727502988
NM_001943.5(DSG2):c.1781T>C (p.Leu594Pro) rs199681901
NM_001943.5(DSG2):c.1791C>T (p.Ser597=) rs768167385
NM_001943.5(DSG2):c.1808A>G (p.Gln603Arg) rs794728080
NM_001943.5(DSG2):c.1851C>T (p.Leu617=) rs202057770
NM_001943.5(DSG2):c.1875G>C (p.Leu625=) rs35743180
NM_001943.5(DSG2):c.1911C>T (p.Cys637=) rs201654341
NM_001943.5(DSG2):c.1914A>G (p.Gly638=) rs200395484
NM_001943.5(DSG2):c.1920C>T (p.Gly640=) rs775642244
NM_001943.5(DSG2):c.2001+20A>G rs746383404
NM_001943.5(DSG2):c.2085G>A (p.Thr695=) rs554396523
NM_001943.5(DSG2):c.2100C>T (p.Ser700=) rs397516704
NM_001943.5(DSG2):c.2112T>G (p.Ile704Met) rs794728081
NM_001943.5(DSG2):c.2127T>C (p.His709=) rs876657457
NM_001943.5(DSG2):c.216+14_216+15del rs876657458
NM_001943.5(DSG2):c.216+20A>C rs762768999
NM_001943.5(DSG2):c.221A>G (p.His74Arg) rs201855245
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.2241C>T (p.Thr747=) rs767628208
NM_001943.5(DSG2):c.2334+9G>A rs776516070
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.2470C>T (p.Arg824Cys) rs201845396
NM_001943.5(DSG2):c.2583A>G (p.Thr861=) rs774775322
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.273A>G (p.Gly91=) rs376944801
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.2759T>G (p.Val920Gly) rs142841727
NM_001943.5(DSG2):c.2880C>G (p.Ser960Arg) rs374807974
NM_001943.5(DSG2):c.2886T>G (p.Ile962Met) rs79229040
NM_001943.5(DSG2):c.291A>C (p.Pro97=) rs727502983
NM_001943.5(DSG2):c.3056G>A (p.Arg1019Lys) rs1057520867
NM_001943.5(DSG2):c.3082G>A (p.Gly1028Ser) rs150864240
NM_001943.5(DSG2):c.3118G>A (p.Val1040Ile) rs201966605
NM_001943.5(DSG2):c.3195T>C (p.Thr1065=) rs544981484
NM_001943.5(DSG2):c.3198A>G (p.Glu1066=) rs727504601
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.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.379-3C>T rs376556524
NM_001943.5(DSG2):c.44T>A (p.Leu15Gln) rs372174546
NM_001943.5(DSG2):c.46-11T>C rs757891590
NM_001943.5(DSG2):c.46-3C>T rs777302616
NM_001943.5(DSG2):c.473T>G (p.Val158Gly) rs191143292
NM_001943.5(DSG2):c.474G>A (p.Val158=) rs397516708
NM_001943.5(DSG2):c.523+20T>C rs775127367
NM_001943.5(DSG2):c.545A>G (p.Asn182Ser) rs368512832
NM_001943.5(DSG2):c.55A>G (p.Asn19Asp) rs185266383
NM_001943.5(DSG2):c.600C>A (p.Ile200=) rs535646295
NM_001943.5(DSG2):c.618T>A (p.Ala206=) rs397516710
NM_001943.5(DSG2):c.6G>A (p.Ala2=) rs368809971
NM_001943.5(DSG2):c.782G>A (p.Arg261His) rs727502984
NM_001943.5(DSG2):c.81+10C>T rs764150806
NM_001943.5(DSG2):c.82-10A>G rs1437170752
NM_001943.5(DSG2):c.828+13C>T rs180926981
NM_001943.5(DSG2):c.829-19_829-18del rs111241096
NM_001943.5(DSG2):c.829-4G>A rs376424003
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.858C>T (p.Val286=) rs1555671463
NM_001943.5(DSG2):c.862G>A (p.Val288Ile) rs780374242
NM_001943.5(DSG2):c.877A>T (p.Ile293Leu) rs2230234
NM_001943.5(DSG2):c.885G>A (p.Val295=) rs534674777
NM_001943.5(DSG2):c.990C>T (p.Asn330=) rs140575919

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