rs796053210

Orientation

plus

Stabilized

plus

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

Make rs796053210(C;T)

Make rs796053210(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

51762666

Gene

SCN8A

is a	snp
is	mentioned by
dbSNP	rs796053210
dbSNP (classic)	rs796053210
ClinGen	rs796053210
ebi	rs796053210
HLI	rs796053210
Exac	rs796053210
Gnomad	rs796053210
Varsome	rs796053210
LitVar	rs796053210
Map	rs796053210
PheGenI	rs796053210
Biobank	rs796053210
1000 genomes	rs796053210
hgdp	rs796053210
ensembl	rs796053210
geneview	rs796053210
scholar	rs796053210
google	rs796053210
pharmgkb	rs796053210
gwascentral	rs796053210
openSNP	rs796053210
23andMe	rs796053210
SNPshot	rs796053210
SNPdbe	rs796053210
MSV3d	rs796053210
GWAS Ctlg	rs796053210

Max Magnitude

0

ClinVar
Risk	rs796053210(T;T)
Alt	rs796053210(T;T)
Reference	Rs796053210(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN8A
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.52156450C>T
CLNSRC
CLNACC	RCV000189266.1,