Human SNP ID | rs7905537 |
---|---|
Human chromosome | chr10 |
Human SNP position | 33942347 |
Pig chromosome | chr10 |
Pig SNP position | 62440055 |
PubMed ID | 20709820 |
---|---|
Journal | Am J Respir Crit Care Med |
Link | www.ncbi.nlm.nih.gov/pubmed/20709820 |
Study | Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema. |
Disease/Trait | Emphysema-related traits |
Initial sample | 2,383 European ancestry cases |
Replication sample | NA |
Region | 10p11.22 |
Chromosome id | chr10 |
Chromosome position | 33942347 |
Reported gene | PARD3 |
Mapped gene | LINC00838 - PARD3 |
Upstream gene id | 100505583 |
Downstream gene id | 56288 |
SNP gene ids | |
Upstream gene distance | 169667 |
Downstream gene distance | 167213 |
SNP risk allele | rs7905537-A |
SNPs | rs7905537 |
Merged | 0 |
SNP id current | 7905537 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.75 |
P value | 0.0000008 |
Pvalue mlog | 6.09691001300805 |
P value text | (quantitative) |
Or beta | 1.85 |
%95 Ci | [NR] HU increase |
Platform | Illumina [499578] |
CNV | N |
Mapped trait | emphysema |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000464 |
Study accession | GCST000770 |