Human SNP ID | rs9268905 |
---|---|
Human chromosome | chr6 |
Human SNP position | 32464300 |
Pig chromosome | chr7 |
Pig SNP position | 29102296 |
PubMed ID | 21602797 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/21602797 |
Study | Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. |
Disease/Trait | Cystic fibrosis severity |
Initial sample | 2,317 European ancestry cases, 177 cases |
Replication sample | 898 European ancestry sibling pair cases, 75 sibling pair cases |
Region | 6p21.32 |
Chromosome id | chr6 |
Chromosome position | 32464300 |
Reported gene | HLA-DRA |
Mapped gene | HLA-DRA - HLA-DRB5 |
Upstream gene id | 3122 |
Downstream gene id | 3127 |
SNP gene ids | |
Upstream gene distance | 19254 |
Downstream gene distance | 53074 |
SNP risk allele | rs9268905-C |
SNPs | rs9268905 |
Merged | 0 |
SNP id current | 9268905 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | 0.32 |
P value | 0.0000001 |
Pvalue mlog | 7 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [~ 2609000] (imputed) |
CNV | N |
Mapped trait | Cystic fibrosis |
Mapped trait URI | http://www.orpha.net/ORDO/Orphanet_586 |
Study accession | GCST001077 |