Human SNP ID | rs4902647 |
---|---|
Human chromosome | chr14 |
Human SNP position | 68787474 |
Pig chromosome | chr7 |
Pig SNP position | 98803197 |
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 | 14q24.1 |
Chromosome id | chr14 |
Chromosome position | 68787474 |
Reported gene | ZFP36L1 |
Mapped gene | RPL12P7 - ZFP36L1 |
Upstream gene id | 326275 |
Downstream gene id | 677 |
SNP gene ids | |
Upstream gene distance | 93848 |
Downstream gene distance | 181 |
SNP risk allele | rs4902647-G |
SNPs | rs4902647 |
Merged | 0 |
SNP id current | 4902647 |
Context | downstream_gene_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000000000009 |
Pvalue mlog | 11.0457574905606 |
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 |