ClinVar Miner

List of variants in gene DSG2 reported as benign

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Gene type:
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Total variants: 82
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HGVS dbSNP
NM_001943.5(DSG2):c.*1339G>A rs9304101
NM_001943.5(DSG2):c.*1866T>C rs1047433
NM_001943.5(DSG2):c.*2C>T rs183494886
NM_001943.5(DSG2):c.*565A>G rs11542765
NM_001943.5(DSG2):c.1014+219G>T rs73416260
NM_001943.5(DSG2):c.1014+266T>C rs9947401
NM_001943.5(DSG2):c.1014+27G>A rs62095194
NM_001943.5(DSG2):c.1015-180C>A rs58713979
NM_001943.5(DSG2):c.1051A>G (p.Ser351Gly) rs139326669
NM_001943.5(DSG2):c.1174G>A (p.Val392Ile) rs193922639
NM_001943.5(DSG2):c.1280+149G>A rs12326068
NM_001943.5(DSG2):c.1280+18G>C rs141175168
NM_001943.5(DSG2):c.1280+234A>G rs10163532
NM_001943.5(DSG2):c.1280+287C>A rs74699553
NM_001943.5(DSG2):c.1280+4AG[3] rs876657791
NM_001943.5(DSG2):c.1303G>A (p.Asp435Asn) rs370509593
NM_001943.5(DSG2):c.1376A>G (p.Tyr459Cys) rs576404380
NM_001943.5(DSG2):c.1491C>T (p.Pro497=) rs587780928
NM_001943.5(DSG2):c.1543G>A (p.Val515Ile) rs2230235
NM_001943.5(DSG2):c.1550C>T (p.Ala517Val) rs200509948
NM_001943.5(DSG2):c.1597G>A (p.Val533Ile) rs199761749
NM_001943.5(DSG2):c.1651+70T>C rs2276150
NM_001943.5(DSG2):c.1652-12C>T rs140850369
NM_001943.5(DSG2):c.1781T>C (p.Leu594Pro) rs199681901
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.1879+317T>C rs1791174
NM_001943.5(DSG2):c.1880-281T>C rs1667212
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.2001+211C>T rs2290128
NM_001943.5(DSG2):c.2001+244G>C rs2290129
NM_001943.5(DSG2):c.2001+308C>T rs7233222
NM_001943.5(DSG2):c.2137G>A (p.Glu713Lys) rs79241126
NM_001943.5(DSG2):c.216+16G>A rs200239610
NM_001943.5(DSG2):c.217-5G>T rs80073511
NM_001943.5(DSG2):c.2211C>T (p.Gly737=) rs74578148
NM_001943.5(DSG2):c.2318G>A (p.Arg773Lys) rs2278792
NM_001943.5(DSG2):c.2334+9G>A rs776516070
NM_001943.5(DSG2):c.2484T>C (p.Asp828=) rs201051252
NM_001943.5(DSG2):c.2505A>G (p.Thr835=) rs1042769
NM_001943.5(DSG2):c.2568A>C (p.Lys856Asn) rs200691513
NM_001943.5(DSG2):c.2586T>C (p.Ser862=) rs78310842
NM_001943.5(DSG2):c.2587A>C (p.Met863Leu) rs16962093
NM_001943.5(DSG2):c.2643C>T (p.Thr881=) rs180695545
NM_001943.5(DSG2):c.2647T>C (p.Ser883Pro) rs34417028
NM_001943.5(DSG2):c.266A>G (p.Tyr89Cys) rs2230232
NM_001943.5(DSG2):c.2703A>G (p.Lys901=) rs113591687
NM_001943.5(DSG2):c.2708C>T (p.Thr903Ile) rs34065672
NM_001943.5(DSG2):c.2759T>G (p.Val920Gly) rs142841727
NM_001943.5(DSG2):c.2886T>G (p.Ile962Met) rs79229040
NM_001943.5(DSG2):c.3082G>A (p.Gly1028Ser) rs150864240
NM_001943.5(DSG2):c.3135A>C (p.Thr1045=) rs8095704
NM_001943.5(DSG2):c.3175T>A (p.Ser1059Thr) rs201786158
NM_001943.5(DSG2):c.3209C>T (p.Thr1070Met) rs149617776
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.3295A>G (p.Thr1099Ala) rs79068489
NM_001943.5(DSG2):c.3321T>C (p.Val1107=) rs1791235
NM_001943.5(DSG2):c.45+257A>C rs9945420
NM_001943.5(DSG2):c.473T>G (p.Val158Gly) rs191143292
NM_001943.5(DSG2):c.523+23_523+24del rs77324780
NM_001943.5(DSG2):c.523+24T>A rs55657337
NM_001943.5(DSG2):c.523+24del
NM_001943.5(DSG2):c.523+252A>G rs62095191
NM_001943.5(DSG2):c.523+9C>T rs587780926
NM_001943.5(DSG2):c.524-243G>C rs2256638
NM_001943.5(DSG2):c.524-9T>A rs11876289
NM_001943.5(DSG2):c.55A>G (p.Asn19Asp) rs185266383
NM_001943.5(DSG2):c.57C>T (p.Asn19=) rs587780925
NM_001943.5(DSG2):c.691-147T>C rs2848664
NM_001943.5(DSG2):c.691-207G>A rs3737375
NM_001943.5(DSG2):c.691-276A>G rs73956201
NM_001943.5(DSG2):c.6G>A (p.Ala2=) rs368809971
NM_001943.5(DSG2):c.81+108C>T rs9807377
NM_001943.5(DSG2):c.81+10C>T rs764150806
NM_001943.5(DSG2):c.81+237A>G rs9807379
NM_001943.5(DSG2):c.81+86G>A rs2276149
NM_001943.5(DSG2):c.828+16C>A rs3737378
NM_001943.5(DSG2):c.852T>C (p.Asn284=) rs62095193
NM_001943.5(DSG2):c.861C>T (p.Asn287=) rs2230233
NM_001943.5(DSG2):c.877A>G (p.Ile293Val) rs2230234

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