rs796053098

Orientation

minus

Stabilized

minus

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

Make rs796053098(A;A)

Make rs796053098(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165992144

Gene	LOC102724058, SCN1A

is a	snp
is	mentioned by
dbSNP	rs796053098
dbSNP (classic)	rs796053098
ClinGen	rs796053098
ebi	rs796053098
HLI	rs796053098
Exac	rs796053098
Gnomad	rs796053098
Varsome	rs796053098
LitVar	rs796053098
Map	rs796053098
PheGenI	rs796053098
Biobank	rs796053098
1000 genomes	rs796053098
hgdp	rs796053098
ensembl	rs796053098
geneview	rs796053098
scholar	rs796053098
google	rs796053098
pharmgkb	rs796053098
gwascentral	rs796053098
openSNP	rs796053098
23andMe	rs796053098
SNPshot	rs796053098
SNPdbe	rs796053098
MSV3d	rs796053098
GWAS Ctlg	rs796053098

Max Magnitude

0

ClinVar
Risk	rs796053098(A;A)
Alt	rs796053098(A;A)
Reference	Rs796053098(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LOC102724058 SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166848654C>T
CLNSRC
CLNACC	RCV000189090.2,