Have questions? Visit https://www.reddit.com/r/SNPedia

rs587780586

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780586(A;A)
Make rs587780586(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position51765675
GeneSCN8A
is asnp
is mentioned by
dbSNPrs587780586
ebirs587780586
HLIrs587780586
Exacrs587780586
Varsomers587780586
Maprs587780586
PheGenIrs587780586
hapmaprs587780586
1000 genomesrs587780586
hgdprs587780586
ensemblrs587780586
gopubmedrs587780586
geneviewrs587780586
scholarrs587780586
googlers587780586
pharmgkbrs587780586
gwascentralrs587780586
openSNPrs587780586
23andMers587780586
23andMe allrs587780586
SNP Nexus

SNPshotrs587780586
SNPdbers587780586
MSV3drs587780586
GWAS Ctlgrs587780586
Max Magnitude0
ClinVar
Risk rs587780586(A;A)
Alt rs587780586(A;A)
Reference rs587780586(G;G)
Significance Pathogenic
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 RCV000122729.2, RCV000189267.2,