List of variants in gene combination SCN1A, SCN9A reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.1642C>T (p.Arg548Ter)	rs1057518900	0.00001
NM_001365536.1(SCN9A):c.1198G>A (p.Val400Met)	rs1553491169
NM_001365536.1(SCN9A):c.2576T>C (p.Ile859Thr)	rs80356474
NM_001365536.1(SCN9A):c.3928G>T (p.Val1310Phe)	rs121908913

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