List of variants in gene SCN7A reported as likely benign 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_002976.4(SCN7A):c.3939G>A (p.Ala1313=)	rs35864629	0.00226
NM_002976.4(SCN7A):c.1479A>G (p.Lys493=)
NM_002976.4(SCN7A):c.2408A>T (p.Asp803Val)	rs148715564
NM_002976.4(SCN7A):c.528C>T (p.Leu176=)
NM_002976.4(SCN7A):c.558C>T (p.Ser186=)

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