rs796052985

Orientation

minus

Stabilized

minus

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

Make rs796052985(C;T)

Make rs796052985(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166037940

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs796052985
dbSNP (classic)	rs796052985
ClinGen	rs796052985
ebi	rs796052985
HLI	rs796052985
Exac	rs796052985
Gnomad	rs796052985
Varsome	rs796052985
LitVar	rs796052985
Map	rs796052985
PheGenI	rs796052985
Biobank	rs796052985
1000 genomes	rs796052985
hgdp	rs796052985
ensembl	rs796052985
geneview	rs796052985
scholar	rs796052985
google	rs796052985
pharmgkb	rs796052985
gwascentral	rs796052985
openSNP	rs796052985
23andMe	rs796052985
SNPshot	rs796052985
SNPdbe	rs796052985
MSV3d	rs796052985
GWAS Ctlg	rs796052985

Max Magnitude

0

ClinVar
Risk	rs796052985(T;T)
Alt	rs796052985(T;T)
Reference	Rs796052985(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166894450G>A
CLNSRC
CLNACC	RCV000188896.1,