ClinVar Miner

List of variants in gene DSC2 reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 51
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HGVS dbSNP
NM_024422.6(DSC2):c.*1017C>T rs191171295
NM_024422.6(DSC2):c.*1096T>C rs74749519
NM_024422.6(DSC2):c.*1104G>A rs186055396
NM_024422.6(DSC2):c.*1126G>T rs886053687
NM_024422.6(DSC2):c.*1158A>G rs749440073
NM_024422.6(DSC2):c.*1183G>A rs886053686
NM_024422.6(DSC2):c.*1237G>A rs28530723
NM_024422.6(DSC2):c.*133G>A rs139923163
NM_024422.6(DSC2):c.*137A>G rs78190086
NM_024422.6(DSC2):c.*1401C>T rs886053685
NM_024422.6(DSC2):c.*1408A>G rs539091896
NM_024422.6(DSC2):c.*1444A>G rs886053684
NM_024422.6(DSC2):c.*1453C>T rs886053683
NM_024422.6(DSC2):c.*1475G>C rs180728052
NM_024422.6(DSC2):c.*1604A>G rs188072930
NM_024422.6(DSC2):c.*1628T>G rs767804423
NM_024422.6(DSC2):c.*166C>G rs886053692
NM_024422.6(DSC2):c.*1704G>T rs181853776
NM_024422.6(DSC2):c.*1784G>T rs375290800
NM_024422.6(DSC2):c.*185A>G rs147458812
NM_024422.6(DSC2):c.*1923C>A rs886053682
NM_024422.6(DSC2):c.*422C>T rs769685892
NM_024422.6(DSC2):c.*46A>T rs77431927
NM_024422.6(DSC2):c.*534A>G rs373266930
NM_024422.6(DSC2):c.*579T>C rs59914360
NM_024422.6(DSC2):c.*640G>T rs886053691
NM_024422.6(DSC2):c.*705G>A rs372988931
NM_024422.6(DSC2):c.*709_*710CT[3] rs886053690
NM_024422.6(DSC2):c.*764T>A rs539965523
NM_024422.6(DSC2):c.*764del rs796836744
NM_024422.6(DSC2):c.*764dup rs796836744
NM_024422.6(DSC2):c.*784G>T rs1613246
NM_024422.6(DSC2):c.*833G>C rs886053689
NM_024422.6(DSC2):c.*864G>A rs746780312
NM_024422.6(DSC2):c.*934C>A rs886053688
NM_024422.6(DSC2):c.111A>G (p.Leu37=) rs12954874
NM_024422.6(DSC2):c.1719C>T (p.Asn573=) rs140167653
NM_024422.6(DSC2):c.1788G>A (p.Ala596=) rs146161960
NM_024422.6(DSC2):c.2198C>T (p.Ala733Val) rs886053695
NM_024422.6(DSC2):c.2205G>T (p.Gln735His) rs886053694
NM_024422.6(DSC2):c.2326A>G (p.Ile776Val) rs1893963
NM_024422.6(DSC2):c.2367A>T (p.Gly789=) rs886053693
NM_024422.6(DSC2):c.2393G>A (p.Arg798Gln) rs61731921
NM_024422.6(DSC2):c.2430G>A (p.Arg810=) rs755276378
NM_024422.6(DSC2):c.2446G>A (p.Val816Met) rs377700521
NM_024422.6(DSC2):c.270G>A (p.Glu90=) rs138643506
NM_024422.6(DSC2):c.351A>G (p.Thr117=) rs117812913
NM_024422.6(DSC2):c.743_748del (p.Tyr248_Thr249del) rs776784065
NM_024422.6(DSC2):c.854T>C (p.Ile285Thr) rs199918720
NM_024422.6(DSC2):c.857G>T (p.Gly286Val) rs199682735
NM_024422.6(DSC2):c.942+13_942+15dup rs5823783

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