List of variants in gene SCN1B reported as benign for Generalized epilepsy with febrile seizures plus, type 1

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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.40+15G>T	rs72556351	0.19938
NM_001037.5(SCN1B):c.*86A>C	rs2278996	0.14285
NM_001037.5(SCN1B):c.*42T>C	rs2278995	0.14069
NM_001037.5(SCN1B):c.*6-11C>G	rs28365105	0.05977
NM_001037.5(SCN1B):c.207+14G>A	rs16969924	0.02860
NM_001037.5(SCN1B):c.501T>C (p.Ile167=)	rs16969930	0.01942
NM_001037.5(SCN1B):c.*76G>T	rs367768639	0.00605
NM_001037.5(SCN1B):c.*401G>A	rs72550268	0.00514
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.-27G>C	rs758958222	0.00013

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