ClinVar Miner

List of variants in gene KCNH2 reported as uncertain significance for Arrhythmia

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Total variants: 29
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HGVS dbSNP
NM_172056.2(KCNH2):c.1071G>T (p.Glu357Asp) rs762016259
NM_172056.2(KCNH2):c.1189C>T (p.Arg397Cys) rs1060500663
NM_172056.2(KCNH2):c.1582C>T (p.Arg528Trp) rs864622403
NM_172056.2(KCNH2):c.2131A>G (p.Ile711Val) rs199473532
NM_172056.2(KCNH2):c.227G>T (p.Arg76Leu) rs868054429
NM_172056.2(KCNH2):c.455C>G (p.Thr152Ser) rs794728354
NM_172056.2(KCNH2):c.460T>C (p.Trp154Arg) rs747591865
NM_172056.2(KCNH2):c.77-5C>A rs72549419
NM_172056.2(KCNH2):c.979T>C (p.Tyr327His) rs776431167
NM_172057.2(KCNH2):c.1546C>G (p.Leu516Val) rs1563150352
NM_172057.2(KCNH2):c.1640G>T (p.Arg547Leu) rs199473432
NM_172057.2(KCNH2):c.1645T>G (p.Leu549Val) rs765427343
NM_172057.2(KCNH2):c.1687G>A (p.Gly563Arg) rs199473669
NM_172057.2(KCNH2):c.1738C>G (p.Arg580Gly) rs199473438
NM_172057.2(KCNH2):c.1748C>T (p.Pro583Leu)
NM_172057.2(KCNH2):c.1812G>C (p.Glu604Asp) rs1232364499
NM_172057.2(KCNH2):c.1841G>A (p.Arg614His) rs772977598
NM_172057.2(KCNH2):c.1921A>G (p.Ser641Gly) rs76649554
NM_172057.2(KCNH2):c.1928C>T (p.Thr643Ile) rs149955375
NM_172057.2(KCNH2):c.2087G>A (p.Gly696Asp) rs199473022
NM_172057.2(KCNH2):c.2089G>A (p.Asp697Asn) rs199473023
NM_172057.2(KCNH2):c.2120G>A (p.Arg707His) rs36210421
NM_172057.2(KCNH2):c.2191A>G (p.Met731Val) rs555797304
NM_172057.2(KCNH2):c.2204C>A (p.Pro735Gln) rs199473028
NM_172057.2(KCNH2):c.2209G>A (p.Ala737Thr) rs201382073
NM_172057.2(KCNH2):c.2258C>T (p.Pro753Leu) rs199473545
NM_172057.2(KCNH2):c.2281C>T (p.Pro761Ser) rs1347039291
NM_172057.2(KCNH2):c.2433C>A (p.His811Gln) rs531426751
NM_172057.2(KCNH2):c.2437C>T (p.His813Tyr) rs199473035

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