rs796053169

Orientation

plus

Stabilized

plus

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

Make rs796053169(A;G)

Make rs796053169(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165307846

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053169
dbSNP (classic)	rs796053169
ClinGen	rs796053169
ebi	rs796053169
HLI	rs796053169
Exac	rs796053169
Gnomad	rs796053169
Varsome	rs796053169
LitVar	rs796053169
Map	rs796053169
PheGenI	rs796053169
Biobank	rs796053169
1000 genomes	rs796053169
hgdp	rs796053169
ensembl	rs796053169
geneview	rs796053169
scholar	rs796053169
google	rs796053169
pharmgkb	rs796053169
gwascentral	rs796053169
openSNP	rs796053169
23andMe	rs796053169
SNPshot	rs796053169
SNPdbe	rs796053169
MSV3d	rs796053169
GWAS Ctlg	rs796053169

Max Magnitude

0

ClinVar
Risk	rs796053169(G;G)
Alt	rs796053169(G;G)
Reference	Rs796053169(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166164356A>G
CLNSRC
CLNACC	RCV000189190.2,