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

rs863225295

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225295(G;G)
Make rs863225295(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51765801
GeneSCN8A
is asnp
is mentioned by
dbSNPrs863225295
ebirs863225295
HLIrs863225295
Exacrs863225295
Varsomers863225295
Maprs863225295
PheGenIrs863225295
hapmaprs863225295
1000 genomesrs863225295
hgdprs863225295
ensemblrs863225295
gopubmedrs863225295
geneviewrs863225295
scholarrs863225295
googlers863225295
pharmgkbrs863225295
gwascentralrs863225295
openSNPrs863225295
23andMers863225295
23andMe allrs863225295
SNP Nexus

SNPshotrs863225295
SNPdbers863225295
MSV3drs863225295
GWAS Ctlgrs863225295
Max Magnitude0
ClinVar
Risk rs863225295(G;G)
Alt rs863225295(G;G)
Reference rs863225295(T;T)
Significance Pathogenic
Disease Early infantile epileptic encephalopathy 13
Variation info
Gene SCN8A
CLNDBN Early infantile epileptic encephalopathy 13
Reversed 0
HGVS NC_000012.11:g.52159585T>G
CLNSRC
CLNACC RCV000201939.1,