Human SNP ID | rs1821625 |
---|---|
Human chromosome | chr2 |
Human SNP position | 133472646 |
Pig chromosome | chr15 |
Pig SNP position | 21144192 |
PubMed ID | 23412934 |
---|---|
Journal | Brain |
Link | www.ncbi.nlm.nih.gov/pubmed/23412934 |
Study | A genome-wide association study of brain lesion distribution in multiple sclerosis. |
Disease/Trait | Multiple sclerosis |
Initial sample | 284 European ancestry individuals |
Replication sample | |
Region | 2q21.2 |
Chromosome id | chr2 |
Chromosome position | 133472646 |
Reported gene | NAP5 |
Mapped gene | NCKAP5 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 344148 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1821625-? |
SNPs | rs1821625 |
Merged | 0 |
SNP id current | 1821625 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | (Cluxel size) |
Or beta | |
%95 Ci | |
Platform | Illumina [208975] |
CNV | N |
Mapped trait | multiple sclerosis |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003885 |
Study accession | GCST001860 |