rs796053227

Orientation

plus

Stabilized

plus

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

Make rs796053227(C;T)

Make rs796053227(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

51807041

Gene

SCN8A

is a	snp
is	mentioned by
dbSNP	rs796053227
dbSNP (classic)	rs796053227
ClinGen	rs796053227
ebi	rs796053227
HLI	rs796053227
Exac	rs796053227
Gnomad	rs796053227
Varsome	rs796053227
LitVar	rs796053227
Map	rs796053227
PheGenI	rs796053227
Biobank	rs796053227
1000 genomes	rs796053227
hgdp	rs796053227
ensembl	rs796053227
geneview	rs796053227
scholar	rs796053227
google	rs796053227
pharmgkb	rs796053227
gwascentral	rs796053227
openSNP	rs796053227
23andMe	rs796053227
SNPshot	rs796053227
SNPdbe	rs796053227
MSV3d	rs796053227
GWAS Ctlg	rs796053227

Max Magnitude

0

ClinVar
Risk	rs796053227(T;T)
Alt	rs796053227(T;T)
Reference	Rs796053227(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN8A
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.52200825C>T
CLNSRC
CLNACC	RCV000189288.2,