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

rs12744221

From SNPedia

Orientationminus
Stabilizedminus
Make rs12744221(C;C)
Make rs12744221(C;T)
Make rs12744221(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position145789475
GeneRNF115
is asnp
is mentioned by
dbSNPrs12744221
ebirs12744221
HLIrs12744221
Exacrs12744221
Varsomers12744221
Maprs12744221
PheGenIrs12744221
hapmaprs12744221
1000 genomesrs12744221
hgdprs12744221
ensemblrs12744221
gopubmedrs12744221
geneviewrs12744221
scholarrs12744221
googlers12744221
pharmgkbrs12744221
gwascentralrs12744221
openSNPrs12744221
23andMers12744221
23andMe allrs12744221
SNP Nexus

SNPshotrs12744221
SNPdbers12744221
MSV3drs12744221
GWAS Ctlgrs12744221
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 C
P-val 6E-6
Odds Ratio 1.66 [NR]