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rs10029851

From SNPedia

Orientationplus
Stabilizedplus
Make rs10029851(A;A)
Make rs10029851(A;C)
Make rs10029851(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position108706869
is asnp
is mentioned by
dbSNPrs10029851
ebirs10029851
HLIrs10029851
Exacrs10029851
Varsomers10029851
Maprs10029851
PheGenIrs10029851
hapmaprs10029851
1000 genomesrs10029851
hgdprs10029851
ensemblrs10029851
gopubmedrs10029851
geneviewrs10029851
scholarrs10029851
googlers10029851
pharmgkbrs10029851
gwascentralrs10029851
openSNPrs10029851
23andMers10029851
23andMe allrs10029851
SNP Nexus

SNPshotrs10029851
SNPdbers10029851
MSV3drs10029851
GWAS Ctlgrs10029851
Max Magnitude
? (A;A) (A;C) (C;C) 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