List of variants in gene SEMA6B reported as benign for epilepsy

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_032108.4(SEMA6B):c.307-31T>G	rs10422881	0.79751
NM_032108.4(SEMA6B):c.1601+24C>T	rs4807602	0.54013
NM_032108.4(SEMA6B):c.39G>C (p.Leu13=)	rs2304213	0.42756
NM_032108.4(SEMA6B):c.1454+30G>T	rs10853972	0.40419
NM_032108.4(SEMA6B):c.772-22G>A	rs45579944	0.09881

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