rs796052972

Orientation

minus

Stabilized

minus

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

Make rs796052972(A;A)

Make rs796052972(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166047644

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs796052972
dbSNP (classic)	rs796052972
ClinGen	rs796052972
ebi	rs796052972
HLI	rs796052972
Exac	rs796052972
Gnomad	rs796052972
Varsome	rs796052972
LitVar	rs796052972
Map	rs796052972
PheGenI	rs796052972
Biobank	rs796052972
1000 genomes	rs796052972
hgdp	rs796052972
ensembl	rs796052972
geneview	rs796052972
scholar	rs796052972
google	rs796052972
pharmgkb	rs796052972
gwascentral	rs796052972
openSNP	rs796052972
23andMe	rs796052972
SNPshot	rs796052972
SNPdbe	rs796052972
MSV3d	rs796052972
GWAS Ctlg	rs796052972

Max Magnitude

0

ClinVar
Risk	rs796052972(A;A)
Alt	rs796052972(A;A)
Reference	Rs796052972(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166904154C>T
CLNSRC
CLNACC	RCV000188862.1,