SNP Detail For rs7755729
1.Mapping Information
Human SNP ID rs7755729
Human chromosome chr6
Human SNP position 129462497
Pig chromosome chr1
Pig SNP position 37494573
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
Region6q22.33
Chromosome idchr6
Chromosome position129462497
Reported geneLAMA2
Mapped geneLAMA2
Upstream gene id
Downstream gene id
SNP gene ids3908
Upstream gene distance
Downstream gene distance
SNP risk allelers7755729-?
SNPsrs7755729
Merged0
SNP id current7755729
Contextintron_variant
Intergenic0
Allele frequency
P value0.000003
Pvalue mlog5.52287874528033
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