rs796053065

Orientation

minus

Stabilized

minus

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

Make rs796053065(-;-)

Make rs796053065(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166039443

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs796053065
dbSNP (classic)	rs796053065
ClinGen	rs796053065
ebi	rs796053065
HLI	rs796053065
Exac	rs796053065
Gnomad	rs796053065
Varsome	rs796053065
LitVar	rs796053065
Map	rs796053065
PheGenI	rs796053065
Biobank	rs796053065
1000 genomes	rs796053065
hgdp	rs796053065
ensembl	rs796053065
geneview	rs796053065
scholar	rs796053065
google	rs796053065
pharmgkb	rs796053065
gwascentral	rs796053065
openSNP	rs796053065
23andMe	rs796053065
SNPshot	rs796053065
SNPdbe	rs796053065
MSV3d	rs796053065
GWAS Ctlg	rs796053065

Max Magnitude

0

ClinVar
Risk	rs796053065(-;-)
Alt	rs796053065(-;-)
Reference	Rs796053065(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166895953delC
CLNSRC
CLNACC	RCV000189045.1,