List of variants in gene SCN1B reported as benign by Ambry Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001037.5(SCN1B):c.501T>C (p.Ile167=)	rs16969930	0.01942
NM_001037.5(SCN1B):c.300C>T (p.Asp100=)	rs16969927	0.00539
NM_001037.5(SCN1B):c.351C>T (p.Gly117=)	rs3746255	0.00082
NM_001037.5(SCN1B):c.412G>A (p.Val138Ile)	rs72558029	0.00058
NM_001037.5(SCN1B):c.414C>T (p.Val138=)	rs757116018	0.00003
NM_001037.5(SCN1B):c.492T>C (p.Tyr164=)	rs535042320

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