List of variants in gene SCN8A reported as likely benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001330260.2(SCN8A):c.4122T>A (p.Thr1374=)	rs115623439	0.00531
NM_001330260.2(SCN8A):c.2632C>T (p.Leu878=)	rs372582842	0.00185
NM_001330260.2(SCN8A):c.3822C>T (p.Val1274=)	rs187327463	0.00132
NM_001330260.2(SCN8A):c.1819G>A (p.Ala607Thr)	rs367949317	0.00061
NM_001330260.2(SCN8A):c.2109T>C (p.Val703=)	rs369029348	0.00033
NM_001330260.2(SCN8A):c.4764C>T (p.Phe1588=)	rs200728478	0.00032
NM_001330260.2(SCN8A):c.4748T>C (p.Ile1583Thr)	rs201458257	0.00027
NM_001330260.2(SCN8A):c.2586C>T (p.Asn862=)	rs377396450	0.00014
NM_001330260.2(SCN8A):c.5046C>T (p.Ile1682=)	rs376759643	0.00011
NM_001330260.2(SCN8A):c.4962C>T (p.Ile1654=)	rs766702527	0.00004
NM_001330260.2(SCN8A):c.3957C>T (p.Ala1319=)	rs764790057	0.00003

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