rs796052976

Orientation

minus

Stabilized

minus

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

Make rs796052976(C;T)

Make rs796052976(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166046799

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs796052976
dbSNP (classic)	rs796052976
ClinGen	rs796052976
ebi	rs796052976
HLI	rs796052976
Exac	rs796052976
Gnomad	rs796052976
Varsome	rs796052976
LitVar	rs796052976
Map	rs796052976
PheGenI	rs796052976
Biobank	rs796052976
1000 genomes	rs796052976
hgdp	rs796052976
ensembl	rs796052976
geneview	rs796052976
scholar	rs796052976
google	rs796052976
pharmgkb	rs796052976
gwascentral	rs796052976
openSNP	rs796052976
23andMe	rs796052976
SNPshot	rs796052976
SNPdbe	rs796052976
MSV3d	rs796052976
GWAS Ctlg	rs796052976

Max Magnitude

0

ClinVar
Risk	rs796052976(T;T)
Alt	rs796052976(T;T)
Reference	Rs796052976(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166903309G>A
CLNSRC
CLNACC	RCV000188869.1,