rs796053132

Orientation

plus

Stabilized

plus

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

Make rs796053132(A;A)

Make rs796053132(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165374709

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053132
dbSNP (classic)	rs796053132
ClinGen	rs796053132
ebi	rs796053132
HLI	rs796053132
Exac	rs796053132
Gnomad	rs796053132
Varsome	rs796053132
LitVar	rs796053132
Map	rs796053132
PheGenI	rs796053132
Biobank	rs796053132
1000 genomes	rs796053132
hgdp	rs796053132
ensembl	rs796053132
geneview	rs796053132
scholar	rs796053132
google	rs796053132
pharmgkb	rs796053132
gwascentral	rs796053132
openSNP	rs796053132
23andMe	rs796053132
SNPshot	rs796053132
SNPdbe	rs796053132
MSV3d	rs796053132
GWAS Ctlg	rs796053132

Max Magnitude

0

ClinVar
Risk	rs796053132(A;A)
Alt	rs796053132(A;A)
Reference	Rs796053132(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166231219G>A
CLNSRC
CLNACC	RCV000189145.3,