Human SNP ID | rs716595 |
---|---|
Human chromosome | chr10 |
Human SNP position | 110246728 |
Pig chromosome | chr14 |
Pig SNP position | 131573110 |
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 | 10q25.2 |
Chromosome id | chr10 |
Chromosome position | 110246728 |
Reported gene | MXI1 |
Mapped gene | MXI1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 4601 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs716595-? |
SNPs | rs716595 |
Merged | 0 |
SNP id current | 716595 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.08 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
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 |