rs796053049

Orientation

minus

Stabilized

minus

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

Make rs796053049(A;G)

Make rs796053049(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165991469

Gene	LOC102724058, SCN1A

is a	snp
is	mentioned by
dbSNP	rs796053049
dbSNP (classic)	rs796053049
ClinGen	rs796053049
ebi	rs796053049
HLI	rs796053049
Exac	rs796053049
Gnomad	rs796053049
Varsome	rs796053049
LitVar	rs796053049
Map	rs796053049
PheGenI	rs796053049
Biobank	rs796053049
1000 genomes	rs796053049
hgdp	rs796053049
ensembl	rs796053049
geneview	rs796053049
scholar	rs796053049
google	rs796053049
pharmgkb	rs796053049
gwascentral	rs796053049
openSNP	rs796053049
23andMe	rs796053049
SNPshot	rs796053049
SNPdbe	rs796053049
MSV3d	rs796053049
GWAS Ctlg	rs796053049

Max Magnitude

0

ClinVar
Risk	rs796053049(G;G)
Alt	rs796053049(G;G)
Reference	Rs796053049(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LOC102724058 SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166847979T>C
CLNSRC
CLNACC	RCV000189022.1,