List of variants reported as benign for Long QT syndrome 2

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.1956T>C (p.Tyr652=)	rs1137617	0.70278
NM_000238.4(KCNH2):c.1692A>G (p.Leu564=)	rs1805121	0.51247
NM_000238.4(KCNH2):c.1539C>T (p.Phe513=)	rs1805120	0.25427
NM_000238.4(KCNH2):c.2690A>C (p.Lys897Thr)	rs1805123	0.20300
NM_000238.4(KCNH2):c.1809C>T (p.Gly603=)	rs41314375	0.01398
NM_000238.4(KCNH2):c.1332G>A (p.Glu444=)	rs9770044	0.01204
NM_000238.4(KCNH2):c.1558-5C>T	rs114186001	0.00642
NM_000238.4(KCNH2):c.1563C>T (p.Ile521=)	rs143011005	0.00097
NM_000238.4(KCNH2):c.*397T>C	rs41312081	0.00078
NM_000238.4(KCNH2):c.442C>T (p.Arg148Trp)	rs139544114	0.00062
NM_000238.4(KCNH2):c.1039C>T (p.Pro347Ser)	rs138776684	0.00061
NM_000238.4(KCNH2):c.422C>T (p.Pro141Leu)	rs199472864	0.00007
NM_000238.4(KCNH2):c.3112G>A (p.Val1038Met)	rs199473544	0.00006
NM_000238.4(KCNH2):c.*92C>T	rs149750773
NM_000238.4(KCNH2):c.1467C>T (p.Ile489=)	rs740952
NM_000238.4(KCNH2):c.3140G>T (p.Arg1047Leu)	rs36210421
NM_000238.4(KCNH2):c.326T>G (p.Leu109Arg)	rs199473498

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