rs796053209

Orientation

plus

Stabilized

plus

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

Make rs796053209(A;G)

Make rs796053209(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

51702879

Gene

SCN8A

is a	snp
is	mentioned by
dbSNP	rs796053209
dbSNP (classic)	rs796053209
ClinGen	rs796053209
ebi	rs796053209
HLI	rs796053209
Exac	rs796053209
Gnomad	rs796053209
Varsome	rs796053209
LitVar	rs796053209
Map	rs796053209
PheGenI	rs796053209
Biobank	rs796053209
1000 genomes	rs796053209
hgdp	rs796053209
ensembl	rs796053209
geneview	rs796053209
scholar	rs796053209
google	rs796053209
pharmgkb	rs796053209
gwascentral	rs796053209
openSNP	rs796053209
23andMe	rs796053209
SNPshot	rs796053209
SNPdbe	rs796053209
MSV3d	rs796053209
GWAS Ctlg	rs796053209

Max Magnitude

0

ClinVar
Risk	rs796053209(G;G)
Alt	rs796053209(G;G)
Reference	Rs796053209(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN8A
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.52096663A>G
CLNSRC
CLNACC	RCV000189260.2,