List of variants in gene combination SCN1A, SCN9A reported as benign for neuropathy, small fiber

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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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.1287T>A (p.Arg429=)	rs6747673	0.56670
NM_001365536.1(SCN9A):c.*2640G>A	rs13396526	0.43246
NM_001365536.1(SCN9A):c.1118_1119insCA	rs140616949	0.10845
NM_001365536.1(SCN9A):c.*1013C>T	rs16851754	0.10746
NM_001365536.1(SCN9A):c.771_772dup	rs144515054	0.07168
NM_001365536.1(SCN9A):c.*1605del	rs148459420	0.06695
NM_001365536.1(SCN9A):c.*2297A>T	rs75345520	0.06645
NM_001365536.1(SCN9A):c.*1774G>A	rs114843828	0.06441
NM_001365536.1(SCN9A):c.1469G>A (p.Ser490Asn)	rs58022607	0.04393
NM_001365536.1(SCN9A):c.1155G>T (p.Val385=)	rs58465962	0.04390
NM_001365536.1(SCN9A):c.*1492C>G	rs73017542	0.03296
NM_001365536.1(SCN9A):c.5756A>G (p.Asp1919Gly)	rs3750904	0.02756
NM_001365536.1(SCN9A):c.3802-8T>C	rs76550960	0.02091
NM_001365536.1(SCN9A):c.*2540C>T	rs58249489	0.01445
NM_001365536.1(SCN9A):c.3004G>T (p.Val1002Leu)	rs4369876	0.01322
NM_001365536.1(SCN9A):c.3675C>A (p.Ile1225=)	rs77144869	0.00141
NM_001365536.1(SCN9A):c.*1660G>A	rs16851753
NM_001365536.1(SCN9A):c.*2154C>G	rs17804037
NM_001365536.1(SCN9A):c.*237C>G	rs16851755
NM_001365536.1(SCN9A):c.244_247dup	rs143461219
NM_001365536.1(SCN9A):c.2616_2626del	rs145255931
NM_001365536.1(SCN9A):c.*416dup	rs3834910
NM_001365536.1(SCN9A):c.529_530del	rs140024416
NM_001365536.1(SCN9A):c.*798dup	rs564394161
NM_001365536.1(SCN9A):c.1975-3dup	rs35888674
NM_001365536.1(SCN9A):c.2874+13del	rs200434162
NM_001365536.1(SCN9A):c.4399-10_4399-7del	rs77944059

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