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

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser)	rs141268327	0.00496
NM_001365536.1(SCN9A):c.5779C>T (p.Leu1927Phe)	rs111558968	0.00315
NM_001365536.1(SCN9A):c.3361C>T (p.Arg1121Trp)	rs190664764	0.00285
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val)	rs182650126	0.00270
NM_001365536.1(SCN9A):c.4645T>C (p.Trp1549Arg)	rs202084411	0.00190
NM_001365536.1(SCN9A):c.2766C>T (p.Arg922=)	rs199653503	0.00088
NM_001365536.1(SCN9A):c.2964C>T (p.Leu988=)	rs201430964	0.00035
NM_001365536.1(SCN9A):c.4953C>G (p.Leu1651=)	rs776545037	0.00001

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