rs796053029

Orientation

minus

Stabilized

minus

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

Make rs796053029(C;C)

Make rs796053029(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165992359

Gene	LOC102724058, SCN1A

is a	snp
is	mentioned by
dbSNP	rs796053029
dbSNP (classic)	rs796053029
ClinGen	rs796053029
ebi	rs796053029
HLI	rs796053029
Exac	rs796053029
Gnomad	rs796053029
Varsome	rs796053029
LitVar	rs796053029
Map	rs796053029
PheGenI	rs796053029
Biobank	rs796053029
1000 genomes	rs796053029
hgdp	rs796053029
ensembl	rs796053029
geneview	rs796053029
scholar	rs796053029
google	rs796053029
pharmgkb	rs796053029
gwascentral	rs796053029
openSNP	rs796053029
23andMe	rs796053029
SNPshot	rs796053029
SNPdbe	rs796053029
MSV3d	rs796053029
GWAS Ctlg	rs796053029

Max Magnitude

0

ClinVar
Risk	rs796053029(C;C)
Alt	rs796053029(C;C)
Reference	Rs796053029(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	LOC102724058 SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166848869C>G
CLNSRC
CLNACC	RCV000188984.2,