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

rs11744876

From SNPedia

Orientationplus
Stabilizedplus
Make rs11744876(A;A)
Make rs11744876(A;G)
Make rs11744876(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position11084600
GeneCTNND2
is asnp
is mentioned by
dbSNPrs11744876
ebirs11744876
HLIrs11744876
Exacrs11744876
Varsomers11744876
Maprs11744876
PheGenIrs11744876
hapmaprs11744876
1000 genomesrs11744876
hgdprs11744876
ensemblrs11744876
gopubmedrs11744876
geneviewrs11744876
scholarrs11744876
googlers11744876
pharmgkbrs11744876
gwascentralrs11744876
openSNPrs11744876
23andMers11744876
23andMe allrs11744876
SNP Nexus

SNPshotrs11744876
SNPdbers11744876
MSV3drs11744876
GWAS Ctlgrs11744876
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-8
Odds Ratio NR NR