rs796052958

Orientation

minus

Stabilized

minus

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

Make rs796052958(A;A)

Make rs796052958(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

166054638

Gene

SCN1A

is a	snp
is	mentioned by
dbSNP	rs796052958
dbSNP (classic)	rs796052958
ClinGen	rs796052958
ebi	rs796052958
HLI	rs796052958
Exac	rs796052958
Gnomad	rs796052958
Varsome	rs796052958
LitVar	rs796052958
Map	rs796052958
PheGenI	rs796052958
Biobank	rs796052958
1000 genomes	rs796052958
hgdp	rs796052958
ensembl	rs796052958
geneview	rs796052958
scholar	rs796052958
google	rs796052958
pharmgkb	rs796052958
gwascentral	rs796052958
openSNP	rs796052958
23andMe	rs796052958
SNPshot	rs796052958
SNPdbe	rs796052958
MSV3d	rs796052958
GWAS Ctlg	rs796052958

Max Magnitude

0

ClinVar
Risk	rs796052958(A;A)
Alt	rs796052958(A;A)
Reference	Rs796052958(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.166911148G>T
CLNSRC
CLNACC	RCV000188836.1,