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rs72698613

From SNPedia

Orientationplus
Stabilizedplus
Make rs72698613(A;A)
Make rs72698613(A;G)
Make rs72698613(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position175087067
is asnp
is mentioned by
dbSNPrs72698613
ebirs72698613
HLIrs72698613
Exacrs72698613
Varsomers72698613
Maprs72698613
PheGenIrs72698613
hapmaprs72698613
1000 genomesrs72698613
hgdprs72698613
ensemblrs72698613
gopubmedrs72698613
geneviewrs72698613
scholarrs72698613
googlers72698613
pharmgkbrs72698613
gwascentralrs72698613
openSNPrs72698613
23andMers72698613
23andMe allrs72698613
SNP Nexus

SNPshotrs72698613
SNPdbers72698613
MSV3drs72698613
GWAS Ctlgrs72698613
Max Magnitude
GWAS snp
PMID [PMID 23962720OA-icon.png]
Trait Epilepsy (remission after treatment)
Title A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy.
Risk Allele A
P-val 4E-6
Odds Ratio 2.39 [NR]