rs796053001

Orientation

minus

Stabilized

minus

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

Make rs796053001(C;C)

Make rs796053001(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166012138

Gene	LOC102724058, SCN1A

is a	snp
is	mentioned by
dbSNP	rs796053001
dbSNP (classic)	rs796053001
ClinGen	rs796053001
ebi	rs796053001
HLI	rs796053001
Exac	rs796053001
Gnomad	rs796053001
Varsome	rs796053001
LitVar	rs796053001
Map	rs796053001
PheGenI	rs796053001
Biobank	rs796053001
1000 genomes	rs796053001
hgdp	rs796053001
ensembl	rs796053001
geneview	rs796053001
scholar	rs796053001
google	rs796053001
pharmgkb	rs796053001
gwascentral	rs796053001
openSNP	rs796053001
23andMe	rs796053001
SNPshot	rs796053001
SNPdbe	rs796053001
MSV3d	rs796053001
GWAS Ctlg	rs796053001

Max Magnitude

0

ClinVar
Risk	rs796053001(C;C)
Alt	rs796053001(C;C)
Reference	Rs796053001(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LOC102724058 SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166868648A>G
CLNSRC
CLNACC	RCV000188932.1,