ClinVar Miner

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

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Total variants: 44
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HGVS dbSNP
NM_004949.4(DSC2):c.1073C>T (p.Thr358Ile) rs139399951
NM_004949.4(DSC2):c.1901G>A (p.Arg634His) rs200475862
NM_004949.4(DSC2):c.2194T>G (p.Leu732Val) rs151024019
NM_004949.4(DSC2):c.304G>A (p.Glu102Lys) rs144799937
NM_024422.3(DSC2):c.2163G>A (p.Thr721=) rs773220437
NM_024422.4(DSC2):c.1070G>A (p.Arg357His) rs201201194
NM_024422.4(DSC2):c.1077+11G>A rs727504868
NM_024422.4(DSC2):c.1077+9A>T rs369381870
NM_024422.4(DSC2):c.120C>A (p.Pro40=) rs773259822
NM_024422.4(DSC2):c.1264-4G>A rs377439942
NM_024422.4(DSC2):c.1323T>C (p.Ala441=) rs745795354
NM_024422.4(DSC2):c.135C>T (p.Ala45=) rs749323567
NM_024422.4(DSC2):c.1510A>G (p.Ser504Gly) rs750965801
NM_024422.4(DSC2):c.1520+8C>G rs372979057
NM_024422.4(DSC2):c.1521-7C>T rs374810953
NM_024422.4(DSC2):c.172T>G (p.Phe58Val) rs138749562
NM_024422.4(DSC2):c.174T>C (p.Phe58=) rs150792047
NM_024422.4(DSC2):c.1788G>A (p.Ala596=) rs146161960
NM_024422.4(DSC2):c.1789G>T (p.Val597Phe) rs143040393
NM_024422.4(DSC2):c.1914G>C (p.Gln638His) rs147742157
NM_024422.4(DSC2):c.1938T>C (p.Tyr646=) rs397517395
NM_024422.4(DSC2):c.2139G>A (p.Thr713=) rs112532429
NM_024422.4(DSC2):c.2151G>C (p.Gly717=) rs752691135
NM_024422.4(DSC2):c.2157T>C (p.Ser719=) rs985629599
NM_024422.4(DSC2):c.2202G>A (p.Gln734=) rs775922060
NM_024422.4(DSC2):c.2226A>G (p.Thr742=) rs142807209
NM_024422.4(DSC2):c.2250+3A>G rs1555637433
NM_024422.4(DSC2):c.2251-13G>A rs1057523492
NM_024422.4(DSC2):c.2251-20G>A rs779900062
NM_024422.4(DSC2):c.2259G>A (p.Ala753=) rs201086521
NM_024422.4(DSC2):c.2430G>A (p.Arg810=) rs755276378
NM_024422.4(DSC2):c.2442G>A (p.Thr814=) rs750971227
NM_024422.4(DSC2):c.2509-118A>G rs137934790
NM_024422.4(DSC2):c.2509-16T>C rs978907622
NM_024422.4(DSC2):c.285C>T (p.Thr95=) rs773333125
NM_024422.4(DSC2):c.371A>G (p.His124Arg) rs794728061
NM_024422.4(DSC2):c.489G>A (p.Thr163=) rs752952811
NM_024422.4(DSC2):c.630+8_630+10delCTAinsTT rs397517401
NM_024422.4(DSC2):c.70-18T>C rs757641297
NM_024422.4(DSC2):c.70-20G>A rs374486794
NM_024422.4(DSC2):c.741T>C (p.Thr247=) rs1555639671
NM_024422.4(DSC2):c.776-13T>G rs370595433
NM_024422.4(DSC2):c.777C>T (p.Gly259=) rs565694087
NM_024422.4(DSC2):c.870A>G (p.Pro290=) rs142653119

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