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

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: 10

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HGVS	dbSNP
NM_001365536.1(SCN9A):c.1326G>A (p.Ala442=)	rs200065104
NM_001365536.1(SCN9A):c.1469G>A (p.Ser490Asn)	rs58022607
NM_001365536.1(SCN9A):c.2827A>C (p.Met943Leu)	rs12478318
NM_001365536.1(SCN9A):c.2874+11_2874+13delinsTT	rs1553487749
NM_001365536.1(SCN9A):c.3002A>G (p.Tyr1001Cys)	rs199692186
NM_001365536.1(SCN9A):c.3003T>C (p.Tyr1001=)	rs886038521
NM_001365536.1(SCN9A):c.3004G>T (p.Val1002Leu)	rs4369876
NM_001365536.1(SCN9A):c.3402G>T (p.Leu1134Phe)	rs200160858
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser)	rs141268327
NM_001365536.1(SCN9A):c.4314C>T (p.Val1438=)	rs188336294

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