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

rs9568797

From SNPedia

Orientationplus
Stabilizedplus
Make rs9568797(C;C)
Make rs9568797(C;T)
Make rs9568797(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position53039424
GeneOLFM4
is asnp
is mentioned by
dbSNPrs9568797
ebirs9568797
HLIrs9568797
Exacrs9568797
Varsomers9568797
Maprs9568797
PheGenIrs9568797
hapmaprs9568797
1000 genomesrs9568797
hgdprs9568797
ensemblrs9568797
gopubmedrs9568797
geneviewrs9568797
scholarrs9568797
googlers9568797
pharmgkbrs9568797
gwascentralrs9568797
openSNPrs9568797
23andMers9568797
23andMe allrs9568797
SNP Nexus

SNPshotrs9568797
SNPdbers9568797
MSV3drs9568797
GWAS Ctlgrs9568797
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24529757]
Trait Amyotrophic lateral sclerosis (sporadic)
Title A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Risk Allele
P-val 1E-7
Odds Ratio NR NR