ClinVar Miner

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

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Total variants: 27
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HGVS dbSNP
NM_001943.5(DSG2):c.1014+219G>T rs73416260
NM_001943.5(DSG2):c.1014+266T>C rs9947401
NM_001943.5(DSG2):c.1015-180C>A rs58713979
NM_001943.5(DSG2):c.1280+149G>A rs12326068
NM_001943.5(DSG2):c.1280+234A>G rs10163532
NM_001943.5(DSG2):c.1280+287C>A rs74699553
NM_001943.5(DSG2):c.1651+70T>C rs2276150
NM_001943.5(DSG2):c.1879+317T>C rs1791174
NM_001943.5(DSG2):c.1880-281T>C rs1667212
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.2647T>C (p.Ser883Pro) rs34417028
NM_001943.5(DSG2):c.2708C>T (p.Thr903Ile) rs34065672
NM_001943.5(DSG2):c.3209C>T (p.Thr1070Met) rs149617776
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+24T>A rs55657337
NM_001943.5(DSG2):c.523+252A>G rs62095191
NM_001943.5(DSG2):c.524-243G>C rs2256638
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+237A>G rs9807379
NM_001943.5(DSG2):c.81+86G>A rs2276149

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