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rs10458771

From SNPedia

Orientationplus
Stabilizedplus
Make rs10458771(A;A)
Make rs10458771(A;G)
Make rs10458771(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position86402481
is asnp
is mentioned by
dbSNPrs10458771
ebirs10458771
HLIrs10458771
Exacrs10458771
Varsomers10458771
Maprs10458771
PheGenIrs10458771
hapmaprs10458771
1000 genomesrs10458771
hgdprs10458771
ensemblrs10458771
gopubmedrs10458771
geneviewrs10458771
scholarrs10458771
googlers10458771
pharmgkbrs10458771
gwascentralrs10458771
openSNPrs10458771
23andMers10458771
23andMe allrs10458771
SNP Nexus

SNPshotrs10458771
SNPdbers10458771
MSV3drs10458771
GWAS Ctlgrs10458771
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 3E-6
Odds Ratio NR NR