List of variants in gene combination SCN1A, SCN9A reported as benign by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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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.2105-14C>T	rs6432893	0.56480
NM_001365536.1(SCN9A):c.1266A>G (p.Glu422=)	rs13402180	0.38348
NM_001365536.1(SCN9A):c.1119T>C (p.Ala373=)	rs13414203	0.38341
NM_001365536.1(SCN9A):c.2105-15G>A	rs4525717	0.12980
NM_001365536.1(SCN9A):c.3802-4A>G	rs75230218	0.06754
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.5756A>G (p.Asp1919Gly)	rs3750904	0.02756
NM_001365536.1(SCN9A):c.2827A>C (p.Met943Leu)	rs12478318	0.01339
NM_001365536.1(SCN9A):c.3004G>T (p.Val1002Leu)	rs4369876	0.01322
NM_001365536.1(SCN9A):c.1398C>T (p.Ser466=)	rs201531206	0.00386
NM_001365536.1(SCN9A):c.5779C>T (p.Leu1927Phe)	rs111558968	0.00315
NM_001365536.1(SCN9A):c.3361C>T (p.Arg1121Trp)	rs190664764	0.00304
NM_001365536.1(SCN9A):c.4356C>T (p.Phe1452=)	rs201145311	0.00263
NM_001365536.1(SCN9A):c.3506A>C (p.Asn1169Thr)	rs151241025	0.00216
NM_001365536.1(SCN9A):c.3675C>A (p.Ile1225=)	rs77144869	0.00141
NM_001365536.1(SCN9A):c.2409T>C (p.Tyr803=)	rs142219317	0.00106
NM_001365536.1(SCN9A):c.2392A>G (p.Met798Val)	rs149707354	0.00056
NM_001365536.1(SCN9A):c.1828C>A (p.Pro610Thr)	rs41268673
NM_001365536.1(SCN9A):c.1975-3del	rs35888674
NM_001365536.1(SCN9A):c.1975-3dup	rs35888674
NM_001365536.1(SCN9A):c.4399-10_4399-7del	rs77944059

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