ClinVar Miner

List of variants in gene DSC2 reported as likely benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 23
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HGVS dbSNP
NM_004949.4(DSC2):c.1073C>T (p.Thr358Ile) rs139399951
NM_004949.4(DSC2):c.1077+11G>T rs727504868
NM_004949.4(DSC2):c.2194T>G (p.Leu732Val) rs151024019
NM_004949.4(DSC2):c.267G>A (p.Ser89=) rs201363937
NM_004949.4(DSC2):c.702G>A (p.Glu234=) rs397517402
NM_004949.4(DSC2):c.942+13_942+15dupTTA rs5823783
NM_004949.4(DSC2):c.942+16A>T rs111347888
NM_024422.3(DSC2):c.1591A>C (p.Arg531=) rs727502981
NM_024422.3(DSC2):c.1971C>A (p.Gly657=) rs397517396
NM_024422.4(DSC2):c.1521-7C>T rs374810953
NM_024422.4(DSC2):c.1680G>A (p.Thr560=) rs567202599
NM_024422.4(DSC2):c.1776G>A (p.Ala592=) rs727502980
NM_024422.4(DSC2):c.1787C>T (p.Ala596Val) rs148185335
NM_024422.4(DSC2):c.2139G>A (p.Thr713=) rs112532429
NM_024422.4(DSC2):c.2208C>T (p.Asn736=) rs727504534
NM_024422.4(DSC2):c.2497C>T (p.Arg833Cys) rs142410803
NM_024422.4(DSC2):c.2636A>G (p.Asp879Gly) rs143342988
NM_024422.4(DSC2):c.270G>A (p.Glu90=) rs138643506
NM_024422.4(DSC2):c.327A>G (p.Ile109Met) rs373305929
NM_024422.4(DSC2):c.348A>G (p.Gln116=) rs137941742
NM_024422.4(DSC2):c.630+8_630+10delCTAinsTT rs397517401
NM_024422.4(DSC2):c.70-11delT rs572309510
NM_024422.4(DSC2):c.907G>A (p.Val303Met) rs145560678

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