rs587780586

Orientation

plus

Stabilized

plus

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

Make rs587780586(A;A)

Make rs587780586(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

51765675

Gene

SCN8A

is a	snp
is	mentioned by
dbSNP	rs587780586
dbSNP (classic)	rs587780586
ClinGen	rs587780586
ebi	rs587780586
HLI	rs587780586
Exac	rs587780586
Gnomad	rs587780586
Varsome	rs587780586
LitVar	rs587780586
Map	rs587780586
PheGenI	rs587780586
Biobank	rs587780586
1000 genomes	rs587780586
hgdp	rs587780586
ensembl	rs587780586
geneview	rs587780586
scholar	rs587780586
google	rs587780586
pharmgkb	rs587780586
gwascentral	rs587780586
openSNP	rs587780586
23andMe	rs587780586
SNPshot	rs587780586
SNPdbe	rs587780586
MSV3d	rs587780586
GWAS Ctlg	rs587780586

Max Magnitude

0

ClinVar
Risk	rs587780586(A;A)
Alt	rs587780586(A;A)
Reference	Rs587780586(G;G)
Significance	Other
Disease	Early infantile epileptic encephalopathy 13 not provided
Variation	info
Gene	SCN8A
CLNDBN	Early infantile epileptic encephalopathy 13 not provided
Reversed	0
HGVS	NC_000012.11:g.52159459G>A
CLNSRC
CLNACC	RCV000122729.3, RCV000189267.3,