rs796053220

Orientation

plus

Stabilized

plus

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

Make rs796053220(C;T)

Make rs796053220(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

51790450

Gene

SCN8A

is a	snp
is	mentioned by
dbSNP	rs796053220
dbSNP (classic)	rs796053220
ClinGen	rs796053220
ebi	rs796053220
HLI	rs796053220
Exac	rs796053220
Gnomad	rs796053220
Varsome	rs796053220
LitVar	rs796053220
Map	rs796053220
PheGenI	rs796053220
Biobank	rs796053220
1000 genomes	rs796053220
hgdp	rs796053220
ensembl	rs796053220
geneview	rs796053220
scholar	rs796053220
google	rs796053220
pharmgkb	rs796053220
gwascentral	rs796053220
openSNP	rs796053220
23andMe	rs796053220
SNPshot	rs796053220
SNPdbe	rs796053220
MSV3d	rs796053220
GWAS Ctlg	rs796053220

Max Magnitude

0

ClinVar
Risk	rs796053220(T;T)
Alt	rs796053220(T;T)
Reference	Rs796053220(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN8A
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.52184234C>T
CLNSRC
CLNACC	RCV000189281.2,