Human SNP ID | rs1032355 |
---|---|
Human chromosome | chr4 |
Human SNP position | 99618739 |
Pig chromosome | chr8 |
Pig SNP position | 130041868 |
PubMed ID | 23936387 |
---|---|
Journal | PLoS One |
Link | www.ncbi.nlm.nih.gov/pubmed/23936387 |
Study | A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. |
Disease/Trait | Celiac disease |
Initial sample | 206 European ancestry trios |
Replication sample | NA |
Region | 4q23 |
Chromosome id | chr4 |
Chromosome position | 99618739 |
Reported gene | RG9MTD2, C4orf17, MTTP |
Mapped gene | MTTP |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 4547 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1032355-C |
SNPs | rs1032355 |
Merged | 0 |
SNP id current | 1032355 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [944512] (imputed) |
CNV | N |
Mapped trait | celiac disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0001060 |
Study accession | GCST002112 |