rs796053171

Orientation

plus

Stabilized

plus

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

Make rs796053171(G;T)

Make rs796053171(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

165308795

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053171
dbSNP (classic)	rs796053171
ClinGen	rs796053171
ebi	rs796053171
HLI	rs796053171
Exac	rs796053171
Gnomad	rs796053171
Varsome	rs796053171
LitVar	rs796053171
Map	rs796053171
PheGenI	rs796053171
Biobank	rs796053171
1000 genomes	rs796053171
hgdp	rs796053171
ensembl	rs796053171
geneview	rs796053171
scholar	rs796053171
google	rs796053171
pharmgkb	rs796053171
gwascentral	rs796053171
openSNP	rs796053171
23andMe	rs796053171
SNPshot	rs796053171
SNPdbe	rs796053171
MSV3d	rs796053171
GWAS Ctlg	rs796053171

Max Magnitude

0

ClinVar
Risk	rs796053171(T;T)
Alt	rs796053171(T;T)
Reference	Rs796053171(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166165305G>T
CLNSRC
CLNACC	RCV000189192.2,