rs796053211

Orientation

plus

Stabilized

plus

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

Make rs796053211(C;C)

Make rs796053211(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

51765768

Gene

SCN8A

is a	snp
is	mentioned by
dbSNP	rs796053211
dbSNP (classic)	rs796053211
ClinGen	rs796053211
ebi	rs796053211
HLI	rs796053211
Exac	rs796053211
Gnomad	rs796053211
Varsome	rs796053211
LitVar	rs796053211
Map	rs796053211
PheGenI	rs796053211
Biobank	rs796053211
1000 genomes	rs796053211
hgdp	rs796053211
ensembl	rs796053211
geneview	rs796053211
scholar	rs796053211
google	rs796053211
pharmgkb	rs796053211
gwascentral	rs796053211
openSNP	rs796053211
23andMe	rs796053211
SNPshot	rs796053211
SNPdbe	rs796053211
MSV3d	rs796053211
GWAS Ctlg	rs796053211

Max Magnitude

0

ClinVar
Risk	rs796053211(C;C)
Alt	rs796053211(C;C)
Reference	Rs796053211(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN8A
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.52159552T>C
CLNSRC
CLNACC	RCV000189268.1,