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rs11590421

From SNPedia

Orientationplus
Stabilizedplus
Make rs11590421(A;A)
Make rs11590421(A;G)
Make rs11590421(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position38528443
is asnp
is mentioned by
dbSNPrs11590421
ebirs11590421
HLIrs11590421
Exacrs11590421
Varsomers11590421
Maprs11590421
PheGenIrs11590421
hapmaprs11590421
1000 genomesrs11590421
hgdprs11590421
ensemblrs11590421
gopubmedrs11590421
geneviewrs11590421
scholarrs11590421
googlers11590421
pharmgkbrs11590421
gwascentralrs11590421
openSNPrs11590421
23andMers11590421
23andMe allrs11590421
SNP Nexus

SNPshotrs11590421
SNPdbers11590421
MSV3drs11590421
GWAS Ctlgrs11590421
Max Magnitude
? (A;A) (A;G) (G;G) 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 2E-7
Odds Ratio NR NR