rs796053052

Orientation

minus

Stabilized

minus

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

Make rs796053052(-;-)

Make rs796053052(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166058585

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs796053052
dbSNP (classic)	rs796053052
ClinGen	rs796053052
ebi	rs796053052
HLI	rs796053052
Exac	rs796053052
Gnomad	rs796053052
Varsome	rs796053052
LitVar	rs796053052
Map	rs796053052
PheGenI	rs796053052
Biobank	rs796053052
1000 genomes	rs796053052
hgdp	rs796053052
ensembl	rs796053052
geneview	rs796053052
scholar	rs796053052
google	rs796053052
pharmgkb	rs796053052
gwascentral	rs796053052
openSNP	rs796053052
23andMe	rs796053052
SNPshot	rs796053052
SNPdbe	rs796053052
MSV3d	rs796053052
GWAS Ctlg	rs796053052

Max Magnitude

0

ClinVar
Risk	rs796053052(-;-)
Alt	rs796053052(-;-)
Reference	Rs796053052(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166915095delT
CLNSRC
CLNACC	RCV000189032.1,