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

rs794726790

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794726790(C;T)
Make rs794726790(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166045189
GeneSCN1A
is asnp
is mentioned by
dbSNPrs794726790
ebirs794726790
HLIrs794726790
Exacrs794726790
Varsomers794726790
Maprs794726790
PheGenIrs794726790
hapmaprs794726790
1000 genomesrs794726790
hgdprs794726790
ensemblrs794726790
gopubmedrs794726790
geneviewrs794726790
scholarrs794726790
googlers794726790
pharmgkbrs794726790
gwascentralrs794726790
openSNPrs794726790
23andMers794726790
23andMe allrs794726790
SNP Nexus

SNPshotrs794726790
SNPdbers794726790
MSV3drs794726790
GWAS Ctlgrs794726790
Max Magnitude0
ClinVar
Risk rs794726790(T;T)
Alt rs794726790(T;T)
Reference rs794726790(C;C)
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.166901699G>A
CLNSRC Peking University
CLNACC RCV000180906.1,