Human SNP ID | rs13333054 |
---|---|
Human chromosome | chr16 |
Human SNP position | 85977427 |
Pig chromosome | chr6 |
Pig SNP position | 3319788 |
PubMed ID | 21833088 |
---|---|
Journal | Nature |
Link | www.ncbi.nlm.nih.gov/pubmed/21833088 |
Study | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
Disease/Trait | Multiple sclerosis |
Initial sample | 9,772 European ancestry cases, 16,849 European ancestry controls |
Replication sample | 4,218 European ancestry cases, 7,296 European ancestry controls |
Region | 16q24.1 |
Chromosome id | chr16 |
Chromosome position | 85977427 |
Reported gene | IRF8 |
Mapped gene | LOC105371388 - LOC105371389 |
Upstream gene id | 105371388 |
Downstream gene id | 105371389 |
SNP gene ids | |
Upstream gene distance | 28245 |
Downstream gene distance | 70392 |
SNP risk allele | rs13333054-A |
SNPs | rs13333054 |
Merged | 0 |
SNP id current | 13333054 |
Context | upstream_gene_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.00000001 |
Pvalue mlog | 8 |
P value text | |
Or beta | 1.11 |
%95 Ci | [1.1-1.13] |
Platform | Illumina [465434] |
CNV | N |
Mapped trait | multiple sclerosis |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003885 |
Study accession | GCST001198 |