rs796053146

Orientation

plus

Stabilized

plus

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

Make rs796053146(C;T)

Make rs796053146(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165389742

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053146
dbSNP (classic)	rs796053146
ClinGen	rs796053146
ebi	rs796053146
HLI	rs796053146
Exac	rs796053146
Gnomad	rs796053146
Varsome	rs796053146
LitVar	rs796053146
Map	rs796053146
PheGenI	rs796053146
Biobank	rs796053146
1000 genomes	rs796053146
hgdp	rs796053146
ensembl	rs796053146
geneview	rs796053146
scholar	rs796053146
google	rs796053146
pharmgkb	rs796053146
gwascentral	rs796053146
openSNP	rs796053146
23andMe	rs796053146
SNPshot	rs796053146
SNPdbe	rs796053146
MSV3d	rs796053146
GWAS Ctlg	rs796053146

Max Magnitude

0

ClinVar
Risk	rs796053146(T;T)
Alt	rs796053146(T;T)
Reference	Rs796053146(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166246252C>T
CLNSRC
CLNACC	RCV000189160.1,