rs796053113

Orientation

plus

Stabilized

plus

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

Make rs796053113(G;T)

Make rs796053113(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165342470

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053113
dbSNP (classic)	rs796053113
ClinGen	rs796053113
ebi	rs796053113
HLI	rs796053113
Exac	rs796053113
Gnomad	rs796053113
Varsome	rs796053113
LitVar	rs796053113
Map	rs796053113
PheGenI	rs796053113
Biobank	rs796053113
1000 genomes	rs796053113
hgdp	rs796053113
ensembl	rs796053113
geneview	rs796053113
scholar	rs796053113
google	rs796053113
pharmgkb	rs796053113
gwascentral	rs796053113
openSNP	rs796053113
23andMe	rs796053113
SNPshot	rs796053113
SNPdbe	rs796053113
MSV3d	rs796053113
GWAS Ctlg	rs796053113

Max Magnitude

0

ClinVar
Risk	rs796053113(T;T)
Alt	rs796053113(T;T)
Reference	Rs796053113(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166198980G>T
CLNSRC
CLNACC	RCV000189115.1,