SNP Detail For rs4482178
1.Mapping Information
Human SNP ID rs4482178
Human chromosome chr13
Human SNP position 85529954
Pig chromosome chr11
Pig SNP position 61754895
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
Region13q31.1
Chromosome idchr13
Chromosome position85529954
Reported geneSLITRK1
Mapped geneLINC00351
Upstream gene id
Downstream gene id
SNP gene ids100874137
Upstream gene distance
Downstream gene distance
SNP risk allelers4482178-?
SNPsrs4482178
Merged0
SNP id current4482178
Contextintron_variant
Intergenic0
Allele frequency
P value0.0000002
Pvalue mlog6.69897000433601
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