rs794727487

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs794727487(-;-)

Make rs794727487(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

19

Position

35033638

Gene

SCN1B

is a	snp
is	mentioned by
dbSNP	rs794727487
dbSNP (classic)	rs794727487
ClinGen	rs794727487
ebi	rs794727487
HLI	rs794727487
Exac	rs794727487
Gnomad	rs794727487
Varsome	rs794727487
LitVar	rs794727487
Map	rs794727487
PheGenI	rs794727487
Biobank	rs794727487
1000 genomes	rs794727487
hgdp	rs794727487
ensembl	rs794727487
geneview	rs794727487
scholar	rs794727487
google	rs794727487
pharmgkb	rs794727487
gwascentral	rs794727487
openSNP	rs794727487
23andMe	rs794727487
SNPshot	rs794727487
SNPdbe	rs794727487
MSV3d	rs794727487
GWAS Ctlg	rs794727487

Max Magnitude

0

ClinVar
Risk	rs794727487(-;-)
Alt	rs794727487(-;-)
Reference	Rs794727487(C;C)
Significance	Pathogenic
Disease	Generalized epilepsy with febrile seizures plus
Variation	info
Gene	SCN1B
CLNDBN	Generalized epilepsy with febrile seizures plus, type 1
Reversed	0
HGVS	NC_000019.9:g.35524542delC
CLNSRC
CLNACC	RCV000177106.1,