rs796053025

Orientation

minus

Stabilized

minus

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

Make rs796053025(A;G)

Make rs796053025(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165994297

Gene	LOC102724058, SCN1A

is a	snp
is	mentioned by
dbSNP	rs796053025
dbSNP (classic)	rs796053025
ClinGen	rs796053025
ebi	rs796053025
HLI	rs796053025
Exac	rs796053025
Gnomad	rs796053025
Varsome	rs796053025
LitVar	rs796053025
Map	rs796053025
PheGenI	rs796053025
Biobank	rs796053025
1000 genomes	rs796053025
hgdp	rs796053025
ensembl	rs796053025
geneview	rs796053025
scholar	rs796053025
google	rs796053025
pharmgkb	rs796053025
gwascentral	rs796053025
openSNP	rs796053025
23andMe	rs796053025
SNPshot	rs796053025
SNPdbe	rs796053025
MSV3d	rs796053025
GWAS Ctlg	rs796053025

Max Magnitude

0

ClinVar
Risk	rs796053025(G;G)
Alt	rs796053025(G;G)
Reference	Rs796053025(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	LOC102724058 SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166850807T>C
CLNSRC
CLNACC	RCV000188971.2,