rs769520392

Orientation

plus

Stabilized

plus

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

Make rs769520392(A;G)

Make rs769520392(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

51706525

Gene

SCN8A

is a	snp
is	mentioned by
dbSNP	rs769520392
dbSNP (classic)	rs769520392
ClinGen	rs769520392
ebi	rs769520392
HLI	rs769520392
Exac	rs769520392
Gnomad	rs769520392
Varsome	rs769520392
LitVar	rs769520392
Map	rs769520392
PheGenI	rs769520392
Biobank	rs769520392
1000 genomes	rs769520392
hgdp	rs769520392
ensembl	rs769520392
geneview	rs769520392
scholar	rs769520392
google	rs769520392
pharmgkb	rs769520392
gwascentral	rs769520392
openSNP	rs769520392
23andMe	rs769520392
SNPshot	rs769520392
SNPdbe	rs769520392
MSV3d	rs769520392
GWAS Ctlg	rs769520392

Max Magnitude

0

ClinVar
Risk	rs769520392(G;G)
Alt	rs769520392(G;G)
Reference	Rs769520392(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCN8A
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.52100309A>G
CLNSRC
CLNACC	RCV000434079.1,