rs796053114

Orientation

plus

Stabilized

plus

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

Make rs796053114(G;G)

Make rs796053114(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165344596

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053114
dbSNP (classic)	rs796053114
ClinGen	rs796053114
ebi	rs796053114
HLI	rs796053114
Exac	rs796053114
Gnomad	rs796053114
Varsome	rs796053114
LitVar	rs796053114
Map	rs796053114
PheGenI	rs796053114
Biobank	rs796053114
1000 genomes	rs796053114
hgdp	rs796053114
ensembl	rs796053114
geneview	rs796053114
scholar	rs796053114
google	rs796053114
pharmgkb	rs796053114
gwascentral	rs796053114
openSNP	rs796053114
23andMe	rs796053114
SNPshot	rs796053114
SNPdbe	rs796053114
MSV3d	rs796053114
GWAS Ctlg	rs796053114

Max Magnitude

0

ClinVar
Risk	rs796053114(G;G)
Alt	rs796053114(G;G)
Reference	Rs796053114(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166201106T>G
CLNSRC
CLNACC	RCV000189116.2,