rs796053115

Orientation

plus

Stabilized

plus

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

Make rs796053115(A;A)

Make rs796053115(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165344627

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053115
dbSNP (classic)	rs796053115
ClinGen	rs796053115
ebi	rs796053115
HLI	rs796053115
Exac	rs796053115
Gnomad	rs796053115
Varsome	rs796053115
LitVar	rs796053115
Map	rs796053115
PheGenI	rs796053115
Biobank	rs796053115
1000 genomes	rs796053115
hgdp	rs796053115
ensembl	rs796053115
geneview	rs796053115
scholar	rs796053115
google	rs796053115
pharmgkb	rs796053115
gwascentral	rs796053115
openSNP	rs796053115
23andMe	rs796053115
SNPshot	rs796053115
SNPdbe	rs796053115
MSV3d	rs796053115
GWAS Ctlg	rs796053115

Max Magnitude

0

ClinVar
Risk	rs796053115(A;A)
Alt	rs796053115(A;A)
Reference	Rs796053115(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166201137G>A
CLNSRC
CLNACC	RCV000189117.1,