rs796053155

Orientation

plus

Stabilized

plus

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

Make rs796053155(A;A)

Make rs796053155(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165388683

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053155
dbSNP (classic)	rs796053155
ClinGen	rs796053155
ebi	rs796053155
HLI	rs796053155
Exac	rs796053155
Gnomad	rs796053155
Varsome	rs796053155
LitVar	rs796053155
Map	rs796053155
PheGenI	rs796053155
Biobank	rs796053155
1000 genomes	rs796053155
hgdp	rs796053155
ensembl	rs796053155
geneview	rs796053155
scholar	rs796053155
google	rs796053155
pharmgkb	rs796053155
gwascentral	rs796053155
openSNP	rs796053155
23andMe	rs796053155
SNPshot	rs796053155
SNPdbe	rs796053155
MSV3d	rs796053155
GWAS Ctlg	rs796053155

Max Magnitude

0

ClinVar
Risk	rs796053155(A;A)
Alt	rs796053155(A;A)
Reference	Rs796053155(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166245193G>A
CLNSRC
CLNACC	RCV000189169.2,