rs796053076

Orientation

minus

Stabilized

minus

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

Make rs796053076(-;-)

Make rs796053076(-;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166073481

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs796053076
dbSNP (classic)	rs796053076
ClinGen	rs796053076
ebi	rs796053076
HLI	rs796053076
Exac	rs796053076
Gnomad	rs796053076
Varsome	rs796053076
LitVar	rs796053076
Map	rs796053076
PheGenI	rs796053076
Biobank	rs796053076
1000 genomes	rs796053076
hgdp	rs796053076
ensembl	rs796053076
geneview	rs796053076
scholar	rs796053076
google	rs796053076
pharmgkb	rs796053076
gwascentral	rs796053076
openSNP	rs796053076
23andMe	rs796053076
SNPshot	rs796053076
SNPdbe	rs796053076
MSV3d	rs796053076
GWAS Ctlg	rs796053076

Max Magnitude

0

ClinVar
Risk	rs796053076(-;-)
Alt	rs796053076(-;-)
Reference	Rs796053076(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166929991delA
CLNSRC
CLNACC	RCV000189056.1,