List of variants in gene combination SCN1A, SCN9A reported as benign by GeneDx

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.4774+16T>A	rs10180721	0.89103
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	0.38234
NM_001365536.1(SCN9A):c.1119T>C (p.Ala373=)	rs13414203	0.38227
NM_001365536.1(SCN9A):c.2105-15G>A	rs4525717	0.13503
NM_001365536.1(SCN9A):c.3802-4A>G	rs75230218	0.06537
NM_001365536.1(SCN9A):c.4812G>T (p.Val1604=)	rs149207258	0.06434
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.3802-8T>C	rs76550960	0.02091
NM_001365536.1(SCN9A):c.2827A>C (p.Met943Leu)	rs12478318	0.01480
NM_001365536.1(SCN9A):c.3004G>T (p.Val1002Leu)	rs4369876	0.01322
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser)	rs141268327	0.00496
NM_001365536.1(SCN9A):c.2517+6C>T	rs145316463	0.00440
NM_001365536.1(SCN9A):c.1398C>T (p.Ser466=)	rs201531206	0.00386
NM_001365536.1(SCN9A):c.3361C>T (p.Arg1121Trp)	rs190664764	0.00285
NM_001365536.1(SCN9A):c.4314C>T (p.Val1438=)	rs188336294	0.00171
NM_001365536.1(SCN9A):c.3675C>A (p.Ile1225=)	rs77144869	0.00141
NM_001365536.1(SCN9A):c.2392A>G (p.Met798Val)	rs149707354	0.00097
NM_001365536.1(SCN9A):c.2437A>G (p.Ser813Gly)	rs201890240	0.00078
NM_001365536.1(SCN9A):c.4315G>A (p.Val1439Ile)	rs149346064	0.00061
NM_001365536.1(SCN9A):c.4923T>C (p.Leu1641=)	rs199550149	0.00042
NM_001365536.1(SCN9A):c.2344-20A>T	rs199905079	0.00018
NM_001365536.1(SCN9A):c.1975-3dup	rs35888674
NM_001365536.1(SCN9A):c.2874+11_2874+13delinsTT	rs1553487749
NM_001365536.1(SCN9A):c.4399-10_4399-7del	rs77944059
NM_001365536.1(SCN9A):c.5118T>C (p.Pro1706=)	rs2106337596
NM_001365536.1(SCN9A):c.5124T>C (p.Leu1708=)	rs2106337580

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