SNP Detail For rs11921451
1.Mapping Information
Human SNP ID rs11921451
Human chromosome chr3
Human SNP position 127068316
Pig chromosome chr13
Pig SNP position 80444449
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
Region3q21.3
Chromosome idchr3
Chromosome position127068316
Reported geneC3orf56
Mapped geneLOC105374092 - C3orf56
Upstream gene id105374092
Downstream gene id285311
SNP gene ids
Upstream gene distance24880
Downstream gene distance124815
SNP risk allelers11921451-?
SNPsrs11921451
Merged0
SNP id current11921451
Contextintergenic_variant
Intergenic1
Allele frequency
P value0.000005
Pvalue mlog5.30102999566398
P value text
Or beta
%95 Ci
PlatformIllumina [859311]
CNVN
Mapped traitsporadic amyotrophic lateral sclerosis
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0001357
Study accessionGCST002337