List of variants in gene SCN10A studied for Brugada syndrome 1

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_006514.4(SCN10A):c.5137A>G (p.Met1713Val)	rs6599241	1.00000
NM_006514.4(SCN10A):c.5657C>T (p.Ala1886Val)	rs142653846	0.00318
NM_006514.4(SCN10A):c.3803G>A (p.Arg1268Gln)	rs138832868	0.00259
NM_006514.4(SCN10A):c.3674T>C (p.Ile1225Thr)	rs139638446	0.00048
NM_006514.4(SCN10A):c.4984G>A (p.Gly1662Ser)	rs151090729	0.00047
NM_006514.4(SCN10A):c.2441G>A (p.Arg814His)	rs139861061	0.00041
NM_006514.4(SCN10A):c.281T>G (p.Val94Gly)	rs202143516	0.00033
NM_006514.4(SCN10A):c.472T>G (p.Tyr158Asp)	rs202192818	0.00033
NM_006514.4(SCN10A):c.599C>T (p.Ala200Val)	rs554062977	0.00011
NM_006514.4(SCN10A):c.599+1G>A	rs75991777	0.00006
NM_006514.4(SCN10A):c.4777A>T (p.Ile1593Phe)	rs762600386	0.00005
NM_006514.4(SCN10A):c.410C>T (p.Thr137Met)	rs148663098	0.00001
NM_006514.4(SCN10A):c.1246AAG[1] (p.Lys417del)	rs758898721
NM_006514.4(SCN10A):c.41G>T (p.Arg14Leu)	rs141207048

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