SNP Detail For rs1032355
1.Mapping Information
Human SNP ID rs1032355
Human chromosome chr4
Human SNP position 99618739
Pig chromosome chr8
Pig SNP position 130041868
2.Annotation Information
PubMed ID23936387
JournalPLoS One
Linkwww.ncbi.nlm.nih.gov/pubmed/23936387
StudyA possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.
Disease/TraitCeliac disease
Initial sample206 European ancestry trios
Replication sampleNA
Region4q23
Chromosome idchr4
Chromosome position99618739
Reported geneRG9MTD2, C4orf17, MTTP
Mapped geneMTTP
Upstream gene id
Downstream gene id
SNP gene ids4547
Upstream gene distance
Downstream gene distance
SNP risk allelers1032355-C
SNPsrs1032355
Merged0
SNP id current1032355
Contextintron_variant
Intergenic0
Allele frequency
P value0.000005
Pvalue mlog5.30102999566398
P value text
Or beta
%95 Ci
PlatformIllumina [944512] (imputed)
CNVN
Mapped traitceliac disease
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0001060
Study accessionGCST002112