ClinVar Miner

List of variants in gene DSC2 reported as likely benign for not provided

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Total variants: 19
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HGVS dbSNP
NC_000018.10:g.31091827del
NM_024422.6(DSC2):c.1073C>T (p.Thr358Ile) rs139399951
NM_024422.6(DSC2):c.1077+33A>G
NM_024422.6(DSC2):c.1350A>G (p.Arg450=) rs144242114
NM_024422.6(DSC2):c.155-222C>T
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.1888+92A>G
NM_024422.6(DSC2):c.1889-36T>C
NM_024422.6(DSC2):c.1914G>C (p.Gln638His) rs147742157
NM_024422.6(DSC2):c.2125+190G>A
NM_024422.6(DSC2):c.2126-239G>T
NM_024422.6(DSC2):c.2392C>A (p.Arg798=) rs201548399
NM_024422.6(DSC2):c.2508+305G>T
NM_024422.6(DSC2):c.2508+309C>T
NM_024422.6(DSC2):c.2509-245A>G
NM_024422.6(DSC2):c.360A>G (p.Leu120=) rs375772629
NM_024422.6(DSC2):c.474+45C>G
NM_024422.6(DSC2):c.775+8C>A

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