ClinVar Miner

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

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Gene type:
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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_001943.5(DSG2):c.861C>T (p.Asn287=) rs2230233 0.50779
NM_001943.5(DSG2):c.1424-255T>A rs2595364 0.48758
NM_001943.5(DSG2):c.3321T>C (p.Val1107=) rs1791235 0.48308
NM_001943.5(DSG2):c.45+257A>C rs9945420 0.40632
NM_001943.5(DSG2):c.81+86G>A rs2276149 0.39540
NM_001943.5(DSG2):c.524-243G>C rs2256638 0.30425
NM_001943.5(DSG2):c.1280+234A>G rs10163532 0.26246
NM_001943.5(DSG2):c.81+237A>G rs9807379 0.23408
NM_001943.5(DSG2):c.1879+317T>C rs1791174 0.23381
NM_001943.5(DSG2):c.81+108C>T rs9807377 0.23214
NM_001943.5(DSG2):c.523+252A>G rs62095191 0.22762
NM_001943.5(DSG2):c.1014+27G>A rs62095194 0.22724
NM_001943.5(DSG2):c.691-207G>A rs3737375 0.22655
NM_001943.5(DSG2):c.828+16C>A rs3737378 0.22345
NM_001943.5(DSG2):c.2318G>A (p.Arg773Lys) rs2278792 0.22185
NM_001943.5(DSG2):c.2001+244G>C rs2290129 0.21370
NM_001943.5(DSG2):c.2001+211C>T rs2290128 0.21348
NM_001943.5(DSG2):c.1880-281T>C rs1667212 0.20010
NM_001943.5(DSG2):c.691-147T>C rs2848664 0.19879
NM_001943.5(DSG2):c.1651+70T>C rs2276150 0.16060
NM_001943.5(DSG2):c.523+24T>A rs55657337 0.15444
NM_001943.5(DSG2):c.1014+266T>C rs9947401 0.12468
NM_001943.5(DSG2):c.1280+149G>A rs12326068 0.11629
NM_001943.5(DSG2):c.690+62_690+66del rs10544776 0.06428
NM_001943.5(DSG2):c.217-65C>G rs2155944 0.06211
NM_001943.5(DSG2):c.691-276A>G rs73956201 0.05675
NM_001943.5(DSG2):c.2137G>A (p.Glu713Lys) rs79241126 0.05477
NM_001943.5(DSG2):c.1280+287C>A rs74699553 0.03651
NM_001943.5(DSG2):c.2001+308C>T rs7233222 0.02990
NM_001943.5(DSG2):c.1015-180C>A rs58713979 0.02754
NM_001943.5(DSG2):c.1014+219G>T rs73416260 0.02562
NM_001943.5(DSG2):c.524-9T>A rs11876289 0.02255
NM_001943.5(DSG2):c.2002-135A>G rs11876979 0.01771
NM_001943.5(DSG2):c.2002-216T>C rs11874168 0.01767
NM_001943.5(DSG2):c.217-5G>T rs80073511 0.01232
NM_001943.5(DSG2):c.3243C>T (p.Val1081=) rs11542379 0.01097
NM_001943.5(DSG2):c.1543G>A (p.Val515Ile) rs2230235 0.00917
NM_001943.5(DSG2):c.3135A>C (p.Thr1045=) rs8095704 0.00801
NM_001943.5(DSG2):c.2587A>C (p.Met863Leu) rs16962093 0.00694
NM_001943.5(DSG2):c.2647T>C (p.Ser883Pro) rs34417028 0.00652
NM_001943.5(DSG2):c.2708C>T (p.Thr903Ile) rs34065672 0.00649
NM_001943.5(DSG2):c.473T>G (p.Val158Gly) rs191143292 0.00550
NM_001943.5(DSG2):c.2759T>G (p.Val920Gly) rs142841727 0.00439
NM_001943.5(DSG2):c.266A>G (p.Tyr89Cys) rs2230232 0.00406
NM_001943.5(DSG2):c.3209C>T (p.Thr1070Met) rs149617776 0.00223
NM_001943.5(DSG2):c.2484T>C (p.Asp828=) rs201051252 0.00217
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.*1530T>C rs15668 0.00126
NM_001943.5(DSG2):c.2703A>G (p.Lys901=) rs113591687 0.00114
NM_001943.5(DSG2):c.1280+17C>T rs199885701 0.00017
NM_001943.5(DSG2):c.783T>A (p.Arg261=) rs369869320 0.00016
NM_001943.5(DSG2):c.1303G>A (p.Asp435Asn) rs370509593 0.00003
NM_001943.5(DSG2):c.1434A>G (p.Arg478=) rs755732646 0.00001
NM_001943.5(DSG2):c.1652-8C>T rs770497608 0.00001
NM_001943.5(DSG2):c.297T>C (p.Phe99=) rs1045965107 0.00001
NM_001943.5(DSG2):c.2334+121del rs10714882
NM_001943.5(DSG2):c.2335-200dup rs146938937
NM_001943.5(DSG2):c.3057A>G (p.Arg1019=) rs2144361237
NM_001943.5(DSG2):c.3210G>T (p.Thr1070=) rs771104963
NM_001943.5(DSG2):c.618T>A (p.Ala206=) rs397516710
NM_001943.5(DSG2):c.81+16_81+17delinsTG rs2144311694
NM_001943.5(DSG2):c.877A>G (p.Ile293Val) rs2230234

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