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

rs7587026

From SNPedia

Orientationplus
Stabilizedplus
Make rs7587026(A;A)
Make rs7587026(A;C)
Make rs7587026(C;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position166122240
GeneLOC101929680, SCN1A
is asnp
is mentioned by
dbSNPrs7587026
ebirs7587026
HLIrs7587026
Exacrs7587026
Varsomers7587026
Maprs7587026
PheGenIrs7587026
hapmaprs7587026
1000 genomesrs7587026
hgdprs7587026
ensemblrs7587026
gopubmedrs7587026
geneviewrs7587026
scholarrs7587026
googlers7587026
pharmgkbrs7587026
gwascentralrs7587026
openSNPrs7587026
23andMers7587026
23andMe allrs7587026
SNP Nexus

SNPshotrs7587026
SNPdbers7587026
MSV3drs7587026
GWAS Ctlgrs7587026
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24014518OA-icon.png]
Trait Mesial temporal lobe epilepsy with hippocampal sclerosis
Title Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Risk Allele A
P-val 4E-8
Odds Ratio 1.24 [1.15-1.34]