SNP Detail For rs2898261
1.Mapping Information
Human SNP ID rs2898261
Human chromosome chr8
Human SNP position 11101029
Pig chromosome chr14
Pig SNP position 15801433
2.Annotation Information
PubMed ID25017104
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25017104
StudyGenome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.
Disease/TraitEosinophilic esophagitis
Initial sample657 European ancestry cases, 9,296 European ancestry controls
Replication sampleNA
Region8p23.1
Chromosome idchr8
Chromosome position11101029
Reported geneXKR6
Mapped geneXKR6
Upstream gene id
Downstream gene id
SNP gene ids286046
Upstream gene distance
Downstream gene distance
SNP risk allelers2898261-C
SNPsrs2898261
Merged0
SNP id current2898261
Contextintron_variant
Intergenic0
Allele frequency0.58
P value0.00000005
Pvalue mlog7.30102999566398
P value text
Or beta1.35
%95 Ci[NR]
PlatformIllumina [1468075]
CNVN
Mapped traiteosinophilic esophagitis
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004232
Study accessionGCST002527