List of variants in gene combination SCN1A, SCN9A reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 20

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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.1266A>G (p.Glu422=)	rs13402180	0.38348
NM_001365536.1(SCN9A):c.1119T>C (p.Ala373=)	rs13414203	0.38341
NM_001365536.1(SCN9A):c.3802-4A>G	rs75230218	0.06754
NM_001365536.1(SCN9A):c.4812G>T (p.Val1604=)	rs149207258	0.06646
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.3802-8T>C	rs76550960	0.02262
NM_001365536.1(SCN9A):c.3362G>A (p.Arg1121Gln)	rs74401238	0.02210
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.3767A>G (p.Asn1256Ser)	rs141268327	0.00496
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val)	rs182650126	0.00278
NM_001365536.1(SCN9A):c.3675C>A (p.Ile1225=)	rs77144869	0.00141
NM_001365536.1(SCN9A):c.3195C>T (p.Ser1065=)	rs111674454	0.00099
NM_001365536.1(SCN9A):c.4923T>C (p.Leu1641=)	rs199550149	0.00041
NM_001365536.1(SCN9A):c.990T>C (p.Cys330=)	rs1384436013	0.00001
NM_001365536.1(SCN9A):c.1828C>A (p.Pro610Thr)	rs41268673
NM_001365536.1(SCN9A):c.2420G>T (p.Gly807Val)	rs1553488264

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