SNP Detail For rs11061269
1.Mapping Information
Human SNP ID rs11061269
Human chromosome chr12
Human SNP position 130971904
Pig chromosome chr14
Pig SNP position 25765826
2.Annotation Information
PubMed ID24529757
JournalNeurobiol Aging
Linkwww.ncbi.nlm.nih.gov/pubmed/24529757
StudyGenome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Disease/TraitAmyotrophic lateral sclerosis (sporadic)
Initial sample250 Han Chinese ancestry cases, 250 Han Chinese ancestry controls
Replication sampleNA
Region12q24.33
Chromosome idchr12
Chromosome position130971904
Reported geneGPR133
Mapped geneADGRD1
Upstream gene id
Downstream gene id
SNP gene ids283383
Upstream gene distance
Downstream gene distance
SNP risk allelers11061269-?
SNPsrs11061269
Merged0
SNP id current11061269
Contextintron_variant
Intergenic0
Allele frequency0.08
P value0.0000000008
Pvalue mlog9.09691001300805
P value text
Or beta3.7761
%95 Ci[2.49-5.74]
PlatformIllumina [859311]
CNVN
Mapped traitsporadic amyotrophic lateral sclerosis
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0001357
Study accessionGCST002337