rs796053135

Orientation

plus

Stabilized

plus

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

Make rs796053135(A;G)

Make rs796053135(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165374748

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053135
dbSNP (classic)	rs796053135
ClinGen	rs796053135
ebi	rs796053135
HLI	rs796053135
Exac	rs796053135
Gnomad	rs796053135
Varsome	rs796053135
LitVar	rs796053135
Map	rs796053135
PheGenI	rs796053135
Biobank	rs796053135
1000 genomes	rs796053135
hgdp	rs796053135
ensembl	rs796053135
geneview	rs796053135
scholar	rs796053135
google	rs796053135
pharmgkb	rs796053135
gwascentral	rs796053135
openSNP	rs796053135
23andMe	rs796053135
SNPshot	rs796053135
SNPdbe	rs796053135
MSV3d	rs796053135
GWAS Ctlg	rs796053135

Max Magnitude

0

ClinVar
Risk	rs796053135(G;G)
Alt	rs796053135(G;G)
Reference	Rs796053135(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166231258A>G
CLNSRC
CLNACC	RCV000189148.2,