rs796053198

Orientation

plus

Stabilized

plus

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

Make rs796053198(-;-)

Make rs796053198(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165310333

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053198
dbSNP (classic)	rs796053198
ClinGen	rs796053198
ebi	rs796053198
HLI	rs796053198
Exac	rs796053198
Gnomad	rs796053198
Varsome	rs796053198
LitVar	rs796053198
Map	rs796053198
PheGenI	rs796053198
Biobank	rs796053198
1000 genomes	rs796053198
hgdp	rs796053198
ensembl	rs796053198
geneview	rs796053198
scholar	rs796053198
google	rs796053198
pharmgkb	rs796053198
gwascentral	rs796053198
openSNP	rs796053198
23andMe	rs796053198
SNPshot	rs796053198
SNPdbe	rs796053198
MSV3d	rs796053198
GWAS Ctlg	rs796053198

Max Magnitude

0

ClinVar
Risk	rs796053198(-;-)
Alt	rs796053198(-;-)
Reference	Rs796053198(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166166843delC
CLNSRC
CLNACC	RCV000189236.1,