List of variants in gene SCN10A reported as likely benign by Fulgent Genetics, Fulgent Genetics

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_006514.4(SCN10A):c.1768G>A (p.Gly590Arg)	rs35332705	0.00371
NM_006514.4(SCN10A):c.4416C>T (p.Ile1472=)	rs144944369	0.00267
NM_006514.4(SCN10A):c.950+17T>C	rs188914048	0.00231
NM_006514.4(SCN10A):c.1138G>A (p.Val380Ile)	rs142276689	0.00055
NM_006514.4(SCN10A):c.4984G>A (p.Gly1662Ser)	rs151090729	0.00047
NM_006514.4(SCN10A):c.1430C>T (p.Pro477Leu)	rs142235256	0.00039
NM_006514.4(SCN10A):c.2106+8C>T	rs368212766	0.00027
NM_006514.4(SCN10A):c.4089+12A>T	rs151164057	0.00019
NM_006514.4(SCN10A):c.2709C>T (p.Asp903=)	rs368637625	0.00016
NM_006514.4(SCN10A):c.2737G>A (p.Ala913Thr)	rs201054824	0.00013
NM_006514.4(SCN10A):c.1277G>A (p.Arg426Gln)	rs143033805	0.00011
NM_006514.4(SCN10A):c.2324C>T (p.Thr775Ile)	rs150501065	0.00003
NM_006514.4(SCN10A):c.1867+8C>T	rs370354229	0.00001
NM_006514.4(SCN10A):c.41G>T (p.Arg14Leu)	rs141207048

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