rs796053121

Orientation

plus

Stabilized

plus

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

Make rs796053121(A;A)

Make rs796053121(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165344688

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053121
dbSNP (classic)	rs796053121
ClinGen	rs796053121
ebi	rs796053121
HLI	rs796053121
Exac	rs796053121
Gnomad	rs796053121
Varsome	rs796053121
LitVar	rs796053121
Map	rs796053121
PheGenI	rs796053121
Biobank	rs796053121
1000 genomes	rs796053121
hgdp	rs796053121
ensembl	rs796053121
geneview	rs796053121
scholar	rs796053121
google	rs796053121
pharmgkb	rs796053121
gwascentral	rs796053121
openSNP	rs796053121
23andMe	rs796053121
SNPshot	rs796053121
SNPdbe	rs796053121
MSV3d	rs796053121
GWAS Ctlg	rs796053121

Max Magnitude

0

ClinVar
Risk	rs796053121(A;A)
Alt	rs796053121(A;A)
Reference	Rs796053121(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	SCN2A
CLNDBN	not specified
Reversed	0
HGVS	NC_000002.11:g.166201198G>A
CLNSRC
CLNACC	RCV000189124.2,