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rs11061269

From SNPedia

Orientationplus
Stabilizedplus
Make rs11061269(A;A)
Make rs11061269(A;G)
Make rs11061269(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position130971904
GeneGPR133
is asnp
is mentioned by
dbSNPrs11061269
ebirs11061269
HLIrs11061269
Exacrs11061269
Varsomers11061269
Maprs11061269
PheGenIrs11061269
hapmaprs11061269
1000 genomesrs11061269
hgdprs11061269
ensemblrs11061269
gopubmedrs11061269
geneviewrs11061269
scholarrs11061269
googlers11061269
pharmgkbrs11061269
gwascentralrs11061269
openSNPrs11061269
23andMers11061269
23andMe allrs11061269
SNP Nexus

SNPshotrs11061269
SNPdbers11061269
MSV3drs11061269
GWAS Ctlgrs11061269
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 8E-10
Odds Ratio 3.78 [2.49-5.74]