ClinVar Miner

List of variants in gene DSC2 reported as uncertain significance by GeneDx

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Total variants: 46
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HGVS dbSNP
NM_024422.6(DSC2):c.1019C>A (p.Thr340Asn) rs757065157
NM_024422.6(DSC2):c.1081G>A (p.Val361Met) rs751810874
NM_024422.6(DSC2):c.1091T>G (p.Val364Gly) rs368089478
NM_024422.6(DSC2):c.1231A>G (p.Lys411Glu) rs560482778
NM_024422.6(DSC2):c.1276G>A (p.Glu426Lys) rs794728076
NM_024422.6(DSC2):c.1352C>T (p.Ser451Leu) rs794728068
NM_024422.6(DSC2):c.1421C>T (p.Pro474Leu) rs776398212
NM_024422.6(DSC2):c.1521-13T>A rs794728069
NM_024422.6(DSC2):c.1576T>G (p.Ser526Ala) rs794728070
NM_024422.6(DSC2):c.1721G>A (p.Ser574Asn) rs150318400
NM_024422.6(DSC2):c.1729A>G (p.Ile577Val) rs201845641
NM_024422.6(DSC2):c.1766T>C (p.Met589Thr) rs201856473
NM_024422.6(DSC2):c.1775C>T (p.Ala592Val) rs140232809
NM_024422.6(DSC2):c.1787C>T (p.Ala596Val) rs148185335
NM_024422.6(DSC2):c.2033C>T (p.Thr678Ile) rs794728062
NM_024422.6(DSC2):c.2038C>A (p.Arg680Ser) rs757253682
NM_024422.6(DSC2):c.2138C>T (p.Thr713Met) rs180863872
NM_024422.6(DSC2):c.2191G>A (p.Asp731Asn) rs762055797
NM_024422.6(DSC2):c.2245A>C (p.Lys749Gln) rs765067237
NM_024422.6(DSC2):c.2287G>A (p.Ala763Thr) rs777004957
NM_024422.6(DSC2):c.2298G>C (p.Gln766His) rs139558481
NM_024422.6(DSC2):c.2314G>A (p.Val772Met) rs146029947
NM_024422.6(DSC2):c.2318G>C (p.Gly773Ala) rs749174176
NM_024422.6(DSC2):c.2335G>A (p.Gly779Arg) rs139290300
NM_024422.6(DSC2):c.2369G>A (p.Gly790Glu) rs1555637241
NM_024422.6(DSC2):c.2381C>T (p.Ser794Leu) rs1617629
NM_024422.6(DSC2):c.2396G>A (p.Gly799Glu) rs794728071
NM_024422.6(DSC2):c.2498G>A (p.Arg833His) rs370325533
NM_024422.6(DSC2):c.2587G>A (p.Gly863Arg) rs147109895
NM_024422.6(DSC2):c.2603C>T (p.Ser868Phe) rs141873745
NM_024422.6(DSC2):c.2623C>T (p.Arg875Ter) rs727504823
NM_024422.6(DSC2):c.2636A>G (p.Asp879Gly) rs143342988
NM_024422.6(DSC2):c.327A>G (p.Ile109Met) rs373305929
NM_024422.6(DSC2):c.356T>A (p.Val119Asp) rs794728074
NM_024422.6(DSC2):c.431T>C (p.Met144Thr) rs794728065
NM_024422.6(DSC2):c.536A>G (p.Asp179Gly) rs760185784
NM_024422.6(DSC2):c.601G>A (p.Val201Ile) rs202058544
NM_024422.6(DSC2):c.734A>C (p.Glu245Ala) rs373201722
NM_024422.6(DSC2):c.737A>G (p.Glu246Gly) rs1057524741
NM_024422.6(DSC2):c.743_748del (p.Tyr248_Thr249del) rs776784065
NM_024422.6(DSC2):c.745A>C (p.Thr249Pro) rs149848359
NM_024422.6(DSC2):c.802A>G (p.Thr268Ala) rs201015785
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.901A>G (p.Thr301Ala) rs576466497
NM_024422.6(DSC2):c.994T>C (p.Tyr332His) rs794728067

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