rs796053064

Orientation

minus

Stabilized

minus

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

Make rs796053064(-;-)

Make rs796053064(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166043860

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs796053064
dbSNP (classic)	rs796053064
ClinGen	rs796053064
ebi	rs796053064
HLI	rs796053064
Exac	rs796053064
Gnomad	rs796053064
Varsome	rs796053064
LitVar	rs796053064
Map	rs796053064
PheGenI	rs796053064
Biobank	rs796053064
1000 genomes	rs796053064
hgdp	rs796053064
ensembl	rs796053064
geneview	rs796053064
scholar	rs796053064
google	rs796053064
pharmgkb	rs796053064
gwascentral	rs796053064
openSNP	rs796053064
23andMe	rs796053064
SNPshot	rs796053064
SNPdbe	rs796053064
MSV3d	rs796053064
GWAS Ctlg	rs796053064

Max Magnitude

0

ClinVar
Risk	rs796053064(-;-)
Alt	rs796053064(-;-)
Reference	Rs796053064(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166900370delG
CLNSRC
CLNACC	RCV000189044.1,