rs796052964

Orientation

minus

Stabilized

minus

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

Make rs796052964(C;T)

Make rs796052964(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166051841

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs796052964
dbSNP (classic)	rs796052964
ClinGen	rs796052964
ebi	rs796052964
HLI	rs796052964
Exac	rs796052964
Gnomad	rs796052964
Varsome	rs796052964
LitVar	rs796052964
Map	rs796052964
PheGenI	rs796052964
Biobank	rs796052964
1000 genomes	rs796052964
hgdp	rs796052964
ensembl	rs796052964
geneview	rs796052964
scholar	rs796052964
google	rs796052964
pharmgkb	rs796052964
gwascentral	rs796052964
openSNP	rs796052964
23andMe	rs796052964
SNPshot	rs796052964
SNPdbe	rs796052964
MSV3d	rs796052964
GWAS Ctlg	rs796052964

Max Magnitude

0

ClinVar
Risk	rs796052964(T;T)
Alt	rs796052964(T;T)
Reference	Rs796052964(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166908351G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000188849.1,