rs796053214

Orientation

plus

Stabilized

plus

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

Make rs796053214(G;T)

Make rs796053214(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

51786554

Gene

SCN8A

is a	snp
is	mentioned by
dbSNP	rs796053214
dbSNP (classic)	rs796053214
ClinGen	rs796053214
ebi	rs796053214
HLI	rs796053214
Exac	rs796053214
Gnomad	rs796053214
Varsome	rs796053214
LitVar	rs796053214
Map	rs796053214
PheGenI	rs796053214
Biobank	rs796053214
1000 genomes	rs796053214
hgdp	rs796053214
ensembl	rs796053214
geneview	rs796053214
scholar	rs796053214
google	rs796053214
pharmgkb	rs796053214
gwascentral	rs796053214
openSNP	rs796053214
23andMe	rs796053214
SNPshot	rs796053214
SNPdbe	rs796053214
MSV3d	rs796053214
GWAS Ctlg	rs796053214

Max Magnitude

0

ClinVar
Risk	rs796053214(T;T)
Alt	rs796053214(T;T)
Reference	Rs796053214(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	SCN8A
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.52180338G>T
CLNSRC
CLNACC	RCV000189275.2,