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

Minimum submission review status:		Collection method:
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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_001037.5(SCN1B):c.207+14G>A	rs16969924	0.02860
NM_001037.5(SCN1B):c.-9C>A	rs66671189	0.00603
NM_001037.5(SCN1B):c.300C>T (p.Asp100=)	rs16969927	0.00539
NM_001037.5(SCN1B):c.267C>T (p.Arg89=)	rs140949982	0.00232
NM_001037.5(SCN1B):c.448+193G>A	rs66876876	0.00227
NM_001037.5(SCN1B):c.448+321G>A	rs72558028	0.00173
NM_001037.5(SCN1B):c.448+112G>A	rs72558026	0.00049
NM_001037.5(SCN1B):c.448+8G>C	rs200222933	0.00006
NM_001037.5(SCN1B):c.207+13C>T	rs373809858
NM_001037.5(SCN1B):c.448+167C>G	rs529053826
NM_199037.3(SCN1B):c.749G>C (p.Arg250Thr)	rs67486287

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