SNP Detail For rs13268726
1.Mapping Information
Human SNP ID rs13268726
Human chromosome chr8
Human SNP position 125000892
Pig chromosome chr4
Pig SNP position 15275369
2.Annotation Information
PubMed ID24931836
JournalAnn Neurol
Linkwww.ncbi.nlm.nih.gov/pubmed/24931836
StudyC9orf72 and UNC13A are shared risk loci for ALS and FTD: A genome-wide meta-analysis.
Disease/TraitAmyotrophic lateral sclerosis
Initial sample4,377 European ancestry cases, 13,017 European ancestry controls
Replication sampleNA
Region8q24.13
Chromosome idchr8
Chromosome position125000892
Reported geneSQLE, KIAA0196, NSMCE2
Mapped geneSQLE
Upstream gene id
Downstream gene id
SNP gene ids6713
Upstream gene distance
Downstream gene distance
SNP risk allelers13268726-?
SNPsrs13268726
Merged0
SNP id current13268726
Contextintron_variant
Intergenic0
Allele frequency0.1
P value0.000005
Pvalue mlog5.30102999566398
P value text
Or beta1.25
%95 Ci[NR]
PlatformIllumina [~ 1400000] (imputed)
CNVN
Mapped traitamyotrophic lateral sclerosis
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000253
Study accessionGCST002509