rs796053099

Orientation

minus

Stabilized

minus

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

Make rs796053099(C;T)

Make rs796053099(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165992107

Gene	LOC102724058, SCN1A

is a	snp
is	mentioned by
dbSNP	rs796053099
dbSNP (classic)	rs796053099
ClinGen	rs796053099
ebi	rs796053099
HLI	rs796053099
Exac	rs796053099
Gnomad	rs796053099
Varsome	rs796053099
LitVar	rs796053099
Map	rs796053099
PheGenI	rs796053099
Biobank	rs796053099
1000 genomes	rs796053099
hgdp	rs796053099
ensembl	rs796053099
geneview	rs796053099
scholar	rs796053099
google	rs796053099
pharmgkb	rs796053099
gwascentral	rs796053099
openSNP	rs796053099
23andMe	rs796053099
SNPshot	rs796053099
SNPdbe	rs796053099
MSV3d	rs796053099
GWAS Ctlg	rs796053099

Max Magnitude

0

ClinVar
Risk	rs796053099(T;T)
Alt	rs796053099(T;T)
Reference	Rs796053099(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LOC102724058 SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166848617G>A
CLNSRC
CLNACC	RCV000189091.2,