Human SNP ID | rs10518025 |
---|---|
Human chromosome | chr4 |
Human SNP position | 67198722 |
Pig chromosome | chr8 |
Pig SNP position | 69333850 |
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 (severity) |
Initial sample | 794 European ancestry cases, 883 European ancestry controls |
Replication sample | NA |
Region | 4q13.2 |
Chromosome id | chr4 |
Chromosome position | 67198722 |
Reported gene | CENPC1 |
Mapped gene | LOC105377262 - LOC100996585 |
Upstream gene id | 105377262 |
Downstream gene id | 100996585 |
SNP gene ids | |
Upstream gene distance | 121337 |
Downstream gene distance | 181942 |
SNP risk allele | rs10518025-? |
SNPs | rs10518025 |
Merged | 0 |
SNP id current | 10518025 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.14 |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
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 | GCST000266 |