List of variants in gene combination SCN1A, SCN9A reported as benign by Athena Diagnostics Inc

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: 16

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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.3481= (p.Trp1161=)	rs6746030	0.12070
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.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.1398C>T (p.Ser466=)	rs201531206	0.00386
NM_001365536.1(SCN9A):c.1997A>G (p.Lys666Arg)	rs121908919	0.00180
NM_001365536.1(SCN9A):c.4315G>A (p.Val1439Ile)	rs149346064	0.00061
NM_001365536.1(SCN9A):c.1828C>A (p.Pro610Thr)	rs41268673
NM_001365536.1(SCN9A):c.1975-3dup	rs35888674
NM_001365536.1(SCN9A):c.4399-10_4399-7del	rs77944059

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