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

rs863225037

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225037(A;A)
Make rs863225037(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991839
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs863225037
ebirs863225037
HLIrs863225037
Exacrs863225037
Varsomers863225037
Maprs863225037
PheGenIrs863225037
hapmaprs863225037
1000 genomesrs863225037
hgdprs863225037
ensemblrs863225037
gopubmedrs863225037
geneviewrs863225037
scholarrs863225037
googlers863225037
pharmgkbrs863225037
gwascentralrs863225037
openSNPrs863225037
23andMers863225037
23andMe allrs863225037
SNP Nexus

SNPshotrs863225037
SNPdbers863225037
MSV3drs863225037
GWAS Ctlgrs863225037
Max Magnitude0
ClinVar
Risk rs863225037(A;A)
Alt rs863225037(A;A)
Reference rs863225037(G;G)
Significance Pathogenic
Disease Severe myoclonic epilepsy in infancy
Variation info
Gene LOC102724058 SCN1A
CLNDBN Severe myoclonic epilepsy in infancy
Reversed 1
HGVS NC_000002.11:g.166848349C>T
CLNSRC Quest Diagnostics
CLNACC RCV000201173.1,