List of variants in gene SCN1B reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001037.5(SCN1B):c.448+100G>T	rs779658201	0.00002
NM_001037.5(SCN1B):c.374G>A (p.Arg125His)	rs759839781	0.00001
NM_001037.5(SCN1B):c.38T>C (p.Leu13Pro)	rs786205834	0.00001
NM_001037.5(SCN1B):c.1A>C (p.Met1Leu)	rs1375857363
NM_001037.5(SCN1B):c.448+135del	rs761070541
NM_001037.5(SCN1B):c.448+189C>T	rs766373298
NM_001037.5(SCN1B):c.448+337G>T	rs369032304

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