rs796053089

Orientation

minus

Stabilized

minus

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

Make rs796053089(C;T)

Make rs796053089(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166058639

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs796053089
dbSNP (classic)	rs796053089
ClinGen	rs796053089
ebi	rs796053089
HLI	rs796053089
Exac	rs796053089
Gnomad	rs796053089
Varsome	rs796053089
LitVar	rs796053089
Map	rs796053089
PheGenI	rs796053089
Biobank	rs796053089
1000 genomes	rs796053089
hgdp	rs796053089
ensembl	rs796053089
geneview	rs796053089
scholar	rs796053089
google	rs796053089
pharmgkb	rs796053089
gwascentral	rs796053089
openSNP	rs796053089
23andMe	rs796053089
SNPshot	rs796053089
SNPdbe	rs796053089
MSV3d	rs796053089
GWAS Ctlg	rs796053089

Max Magnitude

0

ClinVar
Risk	rs796053089(A;A) rs796053089(T;T)
Alt	rs796053089(A;A) rs796053089(T;T)
Reference	Rs796053089(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166915149G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000189071.1,