List of variants in gene SCN1B studied for Generalized epilepsy with febrile seizures plus

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP
NM_001037.5(SCN1B):c.-132C>G	rs886054339
NM_001037.5(SCN1B):c.-27G>C	rs758958222
NM_001037.5(SCN1B):c.-88A>C	rs886054341
NM_001037.5(SCN1B):c.-93G>C	rs886054340
NM_001037.5(SCN1B):c.-95C>T	rs569134158
NM_001037.5(SCN1B):c.-9C>A	rs66671189
NM_001037.5(SCN1B):c.150C>T (p.Asn50=)	rs147073518
NM_001037.5(SCN1B):c.207+14G>A	rs16969924
NM_001037.5(SCN1B):c.28G>A (p.Gly10Ser)	rs72552027
NM_001037.5(SCN1B):c.351C>T (p.Gly117=)	rs3746255
NM_001037.5(SCN1B):c.363C>G (p.Cys121Trp)	rs104894718
NM_001037.5(SCN1B):c.40+15G>T	rs72556351
NM_001037.5(SCN1B):c.412G>A (p.Val138Ile)	rs72558029
NM_001037.5(SCN1B):c.501T>C (p.Ile167=)	rs16969930

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