ClinVar Miner

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

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Total variants: 76
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HGVS dbSNP
NM_024422.6(DSC2):c.1029T>C (p.Ile343=) rs1555639124
NM_024422.6(DSC2):c.1041T>C (p.Asp347=) rs758394251
NM_024422.6(DSC2):c.1070G>A (p.Arg357His) rs201201194
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.1176T>C (p.Asn392=) rs769365346
NM_024422.6(DSC2):c.1269G>A (p.Leu423=) rs376049846
NM_024422.6(DSC2):c.1347A>G (p.Pro449=) rs1157738158
NM_024422.6(DSC2):c.135C>T (p.Ala45=) rs749323567
NM_024422.6(DSC2):c.1374T>A (p.Val458=) rs1295460147
NM_024422.6(DSC2):c.1401G>A (p.Glu467=) rs977781359
NM_024422.6(DSC2):c.144T>G (p.Leu48=) rs1598592489
NM_024422.6(DSC2):c.1452A>G (p.Ala484=) rs1555638690
NM_024422.6(DSC2):c.1520+8C>G rs372979057
NM_024422.6(DSC2):c.1521-7C>T rs374810953
NM_024422.6(DSC2):c.1552G>C (p.Val518Leu) rs397517394
NM_024422.6(DSC2):c.1559T>C (p.Ile520Thr) rs561310777
NM_024422.6(DSC2):c.159C>T (p.Asn53=) rs952701114
NM_024422.6(DSC2):c.1620C>A (p.Ile540=) rs765374888
NM_024422.6(DSC2):c.1638T>C (p.Asn546=) rs145987522
NM_024422.6(DSC2):c.1674A>T (p.Thr558=) rs761048564
NM_024422.6(DSC2):c.1729A>G (p.Ile577Val) rs201845641
NM_024422.6(DSC2):c.172T>G (p.Phe58Val) rs138749562
NM_024422.6(DSC2):c.1750A>G (p.Ile584Val) rs755041461
NM_024422.6(DSC2):c.1775C>T (p.Ala592Val) rs140232809
NM_024422.6(DSC2):c.1776G>A (p.Ala592=) rs727502980
NM_024422.6(DSC2):c.1787C>T (p.Ala596Val) rs148185335
NM_024422.6(DSC2):c.1788G>A (p.Ala596=) rs146161960
NM_024422.6(DSC2):c.1789G>T (p.Val597Phe) rs143040393
NM_024422.6(DSC2):c.1803G>A (p.Glu601=) rs1288832288
NM_024422.6(DSC2):c.1875G>A (p.Leu625=) rs142594406
NM_024422.6(DSC2):c.1888+7A>G rs1555637977
NM_024422.6(DSC2):c.1935A>G (p.Ser645=) rs878855084
NM_024422.6(DSC2):c.1977T>C (p.Ser659=) rs770010850
NM_024422.6(DSC2):c.1981G>A (p.Val661Ile) rs781419827
NM_024422.6(DSC2):c.1990T>C (p.Leu664=) rs747173696
NM_024422.6(DSC2):c.2031C>T (p.Cys677=) rs754488475
NM_024422.6(DSC2):c.2103G>A (p.Leu701=) rs141726394
NM_024422.6(DSC2):c.2125+9T>G rs1555637547
NM_024422.6(DSC2):c.2175A>C (p.Pro725=) rs921649870
NM_024422.6(DSC2):c.2194T>G (p.Leu732Val) rs151024019
NM_024422.6(DSC2):c.2226A>G (p.Thr742=) rs142807209
NM_024422.6(DSC2):c.2244C>T (p.Asp748=) rs886039103
NM_024422.6(DSC2):c.2259G>A (p.Ala753=) rs201086521
NM_024422.6(DSC2):c.2286C>T (p.Gly762=) rs549251334
NM_024422.6(DSC2):c.2379C>A (p.Thr793=) rs773813155
NM_024422.6(DSC2):c.2416C>T (p.Leu806=) rs758409608
NM_024422.6(DSC2):c.2430G>A (p.Arg810=) rs755276378
NM_024422.6(DSC2):c.2442G>C (p.Thr814=) rs750971227
NM_024422.6(DSC2):c.2471C>T (p.Ser824Leu) rs143413607
NM_024422.6(DSC2):c.2498G>A (p.Arg833His) rs370325533
NM_024422.6(DSC2):c.2502T>C (p.Leu834=) rs1598570166
NM_024422.6(DSC2):c.2509-9C>T rs773056962
NM_024422.6(DSC2):c.2541C>T (p.His847=) rs1598569474
NM_024422.6(DSC2):c.2587G>A (p.Gly863Arg) rs147109895
NM_024422.6(DSC2):c.2636A>G (p.Asp879Gly) rs143342988
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.342G>A (p.Glu114=) rs1598591230
NM_024422.6(DSC2):c.348A>G (p.Gln116=) rs137941742
NM_024422.6(DSC2):c.360A>G (p.Leu120=) rs375772629
NM_024422.6(DSC2):c.408A>G (p.Arg136=) rs561653481
NM_024422.6(DSC2):c.429G>C (p.Ser143=) rs542638302
NM_024422.6(DSC2):c.474+5C>T rs397517400
NM_024422.6(DSC2):c.525T>C (p.Gly175=) rs541223771
NM_024422.6(DSC2):c.585G>A (p.Leu195=) rs912124448
NM_024422.6(DSC2):c.630+8C>T rs201147144
NM_024422.6(DSC2):c.70-7T>G rs184341263
NM_024422.6(DSC2):c.72C>A (p.Ile24=) rs757826575
NM_024422.6(DSC2):c.744T>C (p.Tyr248=) rs756495155
NM_024422.6(DSC2):c.750T>C (p.Phe250=) rs781667894
NM_024422.6(DSC2):c.854T>C (p.Ile285Thr) rs199918720
NM_024422.6(DSC2):c.927T>C (p.Ser309=) rs1434821927
NM_024422.6(DSC2):c.936C>T (p.Asp312=) rs1431388251
NM_024422.6(DSC2):c.951C>T (p.Asp317=) rs749810775
NM_024422.6(DSC2):c.978A>G (p.Gln326=) rs1598583853

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