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

rs794726851

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794726851(G;T)
Make rs794726851(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992212
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs794726851
ebirs794726851
HLIrs794726851
Exacrs794726851
Varsomers794726851
Maprs794726851
PheGenIrs794726851
hapmaprs794726851
1000 genomesrs794726851
hgdprs794726851
ensemblrs794726851
gopubmedrs794726851
geneviewrs794726851
scholarrs794726851
googlers794726851
pharmgkbrs794726851
gwascentralrs794726851
openSNPrs794726851
23andMers794726851
23andMe allrs794726851
SNP Nexus

SNPshotrs794726851
SNPdbers794726851
MSV3drs794726851
GWAS Ctlgrs794726851
Max Magnitude0
ClinVar
Risk rs794726851(T;T)
Alt rs794726851(T;T)
Reference rs794726851(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.166848722C>A
CLNSRC Peking University
CLNACC RCV000180982.1,