rs796053218

Orientation

plus

Stabilized

plus

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

Make rs796053218(C;C)

Make rs796053218(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

51790416

Gene

SCN8A

is a	snp
is	mentioned by
dbSNP	rs796053218
dbSNP (classic)	rs796053218
ClinGen	rs796053218
ebi	rs796053218
HLI	rs796053218
Exac	rs796053218
Gnomad	rs796053218
Varsome	rs796053218
LitVar	rs796053218
Map	rs796053218
PheGenI	rs796053218
Biobank	rs796053218
1000 genomes	rs796053218
hgdp	rs796053218
ensembl	rs796053218
geneview	rs796053218
scholar	rs796053218
google	rs796053218
pharmgkb	rs796053218
gwascentral	rs796053218
openSNP	rs796053218
23andMe	rs796053218
SNPshot	rs796053218
SNPdbe	rs796053218
MSV3d	rs796053218
GWAS Ctlg	rs796053218

Max Magnitude

0

ClinVar
Risk	rs796053218(A;A) rs796053218(C;C)
Alt	rs796053218(A;A) rs796053218(C;C)
Reference	Rs796053218(T;T)
Significance	Pathogenic
Disease	not provided not specified
Variation	info
Gene	SCN8A
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000012.11:g.52184200T>A; NC_000012.11:g.52184200T>C
CLNSRC
CLNACC	RCV000420671.1, RCV000189279.1,