Human SNP ID | rs7779014 |
---|---|
Human chromosome | chr7 |
Human SNP position | 76346269 |
Pig chromosome | chr3 |
Pig SNP position | 9893287 |
PubMed ID | 21654844 |
---|---|
Journal | Genes Immun |
Link | www.ncbi.nlm.nih.gov/pubmed/21654844 |
Study | Genome-wide association study of severity in multiple sclerosis. |
Disease/Trait | Multiple sclerosis |
Initial sample | 1,470 European ancestry cases |
Replication sample | NA |
Region | 7q11.23 |
Chromosome id | chr7 |
Chromosome position | 76346269 |
Reported gene | YWHAG |
Mapped gene | YWHAG |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 7532 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7779014-T |
SNPs | rs7779014 |
Merged | 0 |
SNP id current | 7779014 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.2 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (Continuous) |
Or beta | 0.48 |
%95 Ci | [NR] unit increase |
Platform | Affymetrix [2110417] (imputed) |
CNV | N |
Mapped trait | multiple sclerosis |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003885 |
Study accession | GCST001096 |