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

rs794726823

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794726823(G;T)
Make rs794726823(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166037819
GeneSCN1A
is asnp
is mentioned by
dbSNPrs794726823
ebirs794726823
HLIrs794726823
Exacrs794726823
Varsomers794726823
Maprs794726823
PheGenIrs794726823
hapmaprs794726823
1000 genomesrs794726823
hgdprs794726823
ensemblrs794726823
gopubmedrs794726823
geneviewrs794726823
scholarrs794726823
googlers794726823
pharmgkbrs794726823
gwascentralrs794726823
openSNPrs794726823
23andMers794726823
23andMe allrs794726823
SNP Nexus

SNPshotrs794726823
SNPdbers794726823
MSV3drs794726823
GWAS Ctlgrs794726823
Max Magnitude0
ClinVar
Risk rs794726823(T;T)
Alt rs794726823(T;T)
Reference rs794726823(G;G)
Significance Pathogenic
Disease Severe myoclonic epilepsy in infancy
Variation info
Gene SCN1A
CLNDBN Severe myoclonic epilepsy in infancy
Reversed 1
HGVS NC_000002.11:g.166894329C>A
CLNSRC Peking University
CLNACC RCV000180948.1,