rs181327458

Orientation

plus

Stabilized

plus

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

Make rs181327458(C;T)

Make rs181327458(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

165310448

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs181327458
dbSNP (classic)	rs181327458
ClinGen	rs181327458
ebi	rs181327458
HLI	rs181327458
Exac	rs181327458
Gnomad	rs181327458
Varsome	rs181327458
LitVar	rs181327458
Map	rs181327458
PheGenI	rs181327458
Biobank	rs181327458
1000 genomes	rs181327458
hgdp	rs181327458
ensembl	rs181327458
geneview	rs181327458
scholar	rs181327458
google	rs181327458
pharmgkb	rs181327458
gwascentral	rs181327458
openSNP	rs181327458
23andMe	rs181327458
SNPshot	rs181327458
SNPdbe	rs181327458
MSV3d	rs181327458
GWAS Ctlg	rs181327458

Max Magnitude

0

ClinVar
Risk	rs181327458(T;T)
Alt	rs181327458(T;T)
Reference	Rs181327458(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166166958C>T
CLNSRC
CLNACC	RCV000189195.1,