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rs61670327

From SNPedia

Orientationplus
Stabilizedplus
Make rs61670327(A;A)
Make rs61670327(A;G)
Make rs61670327(G;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position3276582
is asnp
is mentioned by
dbSNPrs61670327
ebirs61670327
HLIrs61670327
Exacrs61670327
Varsomers61670327
Maprs61670327
PheGenIrs61670327
hapmaprs61670327
1000 genomesrs61670327
hgdprs61670327
ensemblrs61670327
gopubmedrs61670327
geneviewrs61670327
scholarrs61670327
googlers61670327
pharmgkbrs61670327
gwascentralrs61670327
openSNPrs61670327
23andMers61670327
23andMe allrs61670327
SNP Nexus

SNPshotrs61670327
SNPdbers61670327
MSV3drs61670327
GWAS Ctlgrs61670327
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 7E-7
Odds Ratio 1.72 [NR]