rs796053182

Orientation

plus

Stabilized

plus

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

Make rs796053182(A;G)

Make rs796053182(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165314008

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053182
dbSNP (classic)	rs796053182
ClinGen	rs796053182
ebi	rs796053182
HLI	rs796053182
Exac	rs796053182
Gnomad	rs796053182
Varsome	rs796053182
LitVar	rs796053182
Map	rs796053182
PheGenI	rs796053182
Biobank	rs796053182
1000 genomes	rs796053182
hgdp	rs796053182
ensembl	rs796053182
geneview	rs796053182
scholar	rs796053182
google	rs796053182
pharmgkb	rs796053182
gwascentral	rs796053182
openSNP	rs796053182
23andMe	rs796053182
SNPshot	rs796053182
SNPdbe	rs796053182
MSV3d	rs796053182
GWAS Ctlg	rs796053182

Max Magnitude

0

ClinVar
Risk	rs796053182(G;G)
Alt	rs796053182(G;G)
Reference	Rs796053182(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166170518A>G
CLNSRC
CLNACC	RCV000189208.3,