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rs11921451

From SNPedia

Orientationplus
Stabilizedplus
Make rs11921451(G;G)
Make rs11921451(G;T)
Make rs11921451(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position127068316
is asnp
is mentioned by
dbSNPrs11921451
ebirs11921451
HLIrs11921451
Exacrs11921451
Varsomers11921451
Maprs11921451
PheGenIrs11921451
hapmaprs11921451
1000 genomesrs11921451
hgdprs11921451
ensemblrs11921451
gopubmedrs11921451
geneviewrs11921451
scholarrs11921451
googlers11921451
pharmgkbrs11921451
gwascentralrs11921451
openSNPrs11921451
23andMers11921451
23andMe allrs11921451
SNP Nexus

SNPshotrs11921451
SNPdbers11921451
MSV3drs11921451
GWAS Ctlgrs11921451
Max Magnitude
? (G;G) (G;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 5E-6
Odds Ratio NR NR