rs796053183

Orientation

plus

Stabilized

plus

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

Make rs796053183(A;C)

Make rs796053183(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

165314014

Gene

SCN2A

is a	snp
is	mentioned by
dbSNP	rs796053183
dbSNP (classic)	rs796053183
ClinGen	rs796053183
ebi	rs796053183
HLI	rs796053183
Exac	rs796053183
Gnomad	rs796053183
Varsome	rs796053183
LitVar	rs796053183
Map	rs796053183
PheGenI	rs796053183
Biobank	rs796053183
1000 genomes	rs796053183
hgdp	rs796053183
ensembl	rs796053183
geneview	rs796053183
scholar	rs796053183
google	rs796053183
pharmgkb	rs796053183
gwascentral	rs796053183
openSNP	rs796053183
23andMe	rs796053183
SNPshot	rs796053183
SNPdbe	rs796053183
MSV3d	rs796053183
GWAS Ctlg	rs796053183

Max Magnitude

0

ClinVar
Risk	rs796053183(C;C) rs796053183(G;G)
Alt	rs796053183(C;C) rs796053183(G;G)
Reference	Rs796053183(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN2A
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.166170524A>C; NC_000002.11:g.166170524A>G
CLNSRC
CLNACC	RCV000189209.2, RCV000189210.2,