Human SNP ID | rs9480865 |
---|---|
Human chromosome | chr6 |
Human SNP position | 108595370 |
Pig chromosome | chr1 |
Pig SNP position | 83973169 |
PubMed ID | 19010793 |
---|---|
Journal | Hum Mol Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/19010793 |
Study | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. |
Disease/Trait | Normalized brain volume |
Initial sample | 753 European ancestry cases, 883 European ancestry controls |
Replication sample | NA |
Region | 6q21 |
Chromosome id | chr6 |
Chromosome position | 108595370 |
Reported gene | FOXO3 |
Mapped gene | FOXO3 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 2309 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs9480865-? |
SNPs | rs9480865 |
Merged | 0 |
SNP id current | 9480865 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.16 |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | |
Or beta | |
%95 Ci | [NR] |
Platform | Illumina [551642] |
CNV | N |
Mapped trait | multiple sclerosis |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003885 |
Study accession | GCST000268 |