Human SNP ID | rs7672826 |
---|---|
Human chromosome | chr4 |
Human SNP position | 181478542 |
Pig chromosome | chr15 |
Pig SNP position | 49626409 |
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 | Multiple sclerosis |
Initial sample | 978 European ancestry cases, 883 European ancestry controls |
Replication sample | NA |
Region | 4q34.3 |
Chromosome id | chr4 |
Chromosome position | 181478542 |
Reported gene | MGC45800 |
Mapped gene | LOC105377574 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105377574 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7672826-? |
SNPs | rs7672826 |
Merged | 0 |
SNP id current | 7672826 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | 0.34 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | |
Or beta | 1.37 |
%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 | GCST000269 |