rs796053134

Orientation

plus

Stabilized

plus

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

Make rs796053134(C;C)

Make rs796053134(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165374737

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053134
dbSNP (classic)	rs796053134
ClinGen	rs796053134
ebi	rs796053134
HLI	rs796053134
Exac	rs796053134
Gnomad	rs796053134
Varsome	rs796053134
LitVar	rs796053134
Map	rs796053134
PheGenI	rs796053134
Biobank	rs796053134
1000 genomes	rs796053134
hgdp	rs796053134
ensembl	rs796053134
geneview	rs796053134
scholar	rs796053134
google	rs796053134
pharmgkb	rs796053134
gwascentral	rs796053134
openSNP	rs796053134
23andMe	rs796053134
SNPshot	rs796053134
SNPdbe	rs796053134
MSV3d	rs796053134
GWAS Ctlg	rs796053134

Max Magnitude

0

ClinVar
Risk	rs796053134(C;C)
Alt	rs796053134(C;C)
Reference	Rs796053134(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166231247T>C
CLNSRC
CLNACC	RCV000189147.1,