rs796053222

Orientation

plus

Stabilized

plus

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

Make rs796053222(C;C)

Make rs796053222(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

51806375

Gene

SCN8A

is a	snp
is	mentioned by
dbSNP	rs796053222
dbSNP (classic)	rs796053222
ClinGen	rs796053222
ebi	rs796053222
HLI	rs796053222
Exac	rs796053222
Gnomad	rs796053222
Varsome	rs796053222
LitVar	rs796053222
Map	rs796053222
PheGenI	rs796053222
Biobank	rs796053222
1000 genomes	rs796053222
hgdp	rs796053222
ensembl	rs796053222
geneview	rs796053222
scholar	rs796053222
google	rs796053222
pharmgkb	rs796053222
gwascentral	rs796053222
openSNP	rs796053222
23andMe	rs796053222
SNPshot	rs796053222
SNPdbe	rs796053222
MSV3d	rs796053222
GWAS Ctlg	rs796053222

Max Magnitude

0

ClinVar
Risk	rs796053222(C;C)
Alt	rs796053222(C;C)
Reference	Rs796053222(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN8A
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.52200159T>C
CLNSRC
CLNACC	RCV000189283.1,