List of variants in gene combination SCN1A, SCN9A reported as pathogenic for not provided

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.2719C>T (p.Arg907Trp)	rs202152511	0.00004
NM_001365536.1(SCN9A):c.1567C>T (p.Arg523Ter)	rs202211795	0.00002
NM_001365536.1(SCN9A):c.1642C>T (p.Arg548Ter)	rs1057518900	0.00001
NM_001365536.1(SCN9A):c.5351del (p.Glu1784fs)	rs1553473041	0.00001
NM_001365536.1(SCN9A):c.984C>A (p.Tyr328Ter)	rs121908917	0.00001
NM_001365536.1(SCN9A):c.1185C>G (p.Asn395Lys)	rs80356471
NM_001365536.1(SCN9A):c.1198G>A (p.Val400Met)	rs1553491169
NM_001365536.1(SCN9A):c.2141G>A (p.Trp714Ter)	rs1057518162
NM_001365536.1(SCN9A):c.2395dup (p.Asp799fs)	rs1697325895
NM_001365536.1(SCN9A):c.2576T>C (p.Ile859Thr)	rs80356474
NM_001365536.1(SCN9A):c.3928G>T (p.Val1310Phe)	rs121908913
NM_001365536.1(SCN9A):c.4495C>T (p.Arg1499Ter)	rs187558439
NM_001365536.1(SCN9A):c.4500del (p.Asn1502fs)	rs1693691531
NM_001365536.1(SCN9A):c.4928C>A (p.Ala1643Glu)	rs879253994
NM_001365536.1(SCN9A):c.966-2A>G	rs1553492481

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