SNP Detail For rs6013382
1.Mapping Information
Human SNP ID rs6013382
Human chromosome chr20
Human SNP position 52086094
Pig chromosome chr17
Pig SNP position 59898835
2.Annotation Information
PubMed ID17362836
JournalLancet Neurol
Linkwww.ncbi.nlm.nih.gov/pubmed/17362836
StudyGenome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.
Disease/TraitAmyotrophic lateral sclerosis
Initial sample276 European ancestry cases, 271 European ancestry controls
Replication sampleNA
Region20q13.2
Chromosome idchr20
Chromosome position52086094
Reported geneZFP64
Mapped geneZFP64, LOC105372664
Upstream gene id
Downstream gene id
SNP gene ids55734, 105372664
Upstream gene distance
Downstream gene distance
SNP risk allelers6013382-?
SNPsrs6013382
Merged0
SNP id current6013382
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000005
Pvalue mlog5.30102999566398
P value text
Or beta1.43
%95 Ci[1.11-1.67]
PlatformIllumina [549062]
CNVN
Mapped traitamyotrophic lateral sclerosis
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000253
Study accessionGCST000013