rs796052999

Orientation

minus

Stabilized

minus

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

Make rs796052999(A;A)

Make rs796052999(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166012104

Gene	LOC102724058, SCN1A

is a	snp
is	mentioned by
dbSNP	rs796052999
dbSNP (classic)	rs796052999
ClinGen	rs796052999
ebi	rs796052999
HLI	rs796052999
Exac	rs796052999
Gnomad	rs796052999
Varsome	rs796052999
LitVar	rs796052999
Map	rs796052999
PheGenI	rs796052999
Biobank	rs796052999
1000 genomes	rs796052999
hgdp	rs796052999
ensembl	rs796052999
geneview	rs796052999
scholar	rs796052999
google	rs796052999
pharmgkb	rs796052999
gwascentral	rs796052999
openSNP	rs796052999
23andMe	rs796052999
SNPshot	rs796052999
SNPdbe	rs796052999
MSV3d	rs796052999
GWAS Ctlg	rs796052999

Max Magnitude

0

ClinVar
Risk	rs796052999(A;A)
Alt	rs796052999(A;A)
Reference	Rs796052999(G;G)
Significance	Other
Disease	not provided
Variation	info
Gene	LOC102724058 SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166868614C>T
CLNSRC
CLNACC	RCV000188930.2,