ClinVar Miner

List of variants in gene DSC2 reported as likely benign by Color

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Total variants: 24
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HGVS dbSNP
NM_024422.6(DSC2):c.1073C>T (p.Thr358Ile) rs139399951
NM_024422.6(DSC2):c.1131T>G (p.Thr377=) rs772815380
NM_024422.6(DSC2):c.1521-7C>T rs374810953
NM_024422.6(DSC2):c.153A>G (p.Arg51=) rs781424888
NM_024422.6(DSC2):c.1591A>C (p.Arg531=) rs727502981
NM_024422.6(DSC2):c.174T>C (p.Phe58=) rs150792047
NM_024422.6(DSC2):c.1787C>T (p.Ala596Val) rs148185335
NM_024422.6(DSC2):c.1881A>G (p.Ala627=) rs752023626
NM_024422.6(DSC2):c.2163G>A (p.Thr721=) rs773220437
NM_024422.6(DSC2):c.2194T>G (p.Leu732Val) rs151024019
NM_024422.6(DSC2):c.2286C>T (p.Gly762=) rs549251334
NM_024422.6(DSC2):c.2313C>T (p.Thr771=) rs778571921
NM_024422.6(DSC2):c.2352C>T (p.Ile784=) rs562571453
NM_024422.6(DSC2):c.2497C>T (p.Arg833Cys) rs142410803
NM_024422.6(DSC2):c.2509-95C>T rs781646028
NM_024422.6(DSC2):c.270G>A (p.Glu90=) rs138643506
NM_024422.6(DSC2):c.304G>A (p.Glu102Lys) rs144799937
NM_024422.6(DSC2):c.348A>G (p.Gln116=) rs137941742
NM_024422.6(DSC2):c.474+4C>A rs1567982295
NM_024422.6(DSC2):c.525T>C (p.Gly175=) rs541223771
NM_024422.6(DSC2):c.534T>G (p.Val178=) rs1567981655
NM_024422.6(DSC2):c.627T>C (p.Phe209=) rs754168300
NM_024422.6(DSC2):c.631-13dup rs551337657
NM_024422.6(DSC2):c.907G>A (p.Val303Met) rs145560678

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