Human SNP ID | rs7216389 |
---|---|
Human chromosome | chr17 |
Human SNP position | 39913696 |
Pig chromosome | chr12 |
Pig SNP position | 22883510 |
PubMed ID | 17611496 |
---|---|
Journal | Nature |
Link | www.ncbi.nlm.nih.gov/pubmed/17611496 |
Study | Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. |
Disease/Trait | Asthma |
Initial sample | 994 European ancestry cases, 1,243 European ancestry controls |
Replication sample | 200 European ancestry cases, 2,120 European ancestry controls |
Region | 17q21.1 |
Chromosome id | chr17 |
Chromosome position | 39913696 |
Reported gene | ORMDL3 |
Mapped gene | GSDMB |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 55876 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7216389-T |
SNPs | rs7216389 |
Merged | 0 |
SNP id current | 7216389 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.52 |
P value | 0.00000000009 |
Pvalue mlog | 10.0457574905606 |
P value text | |
Or beta | 1.45 |
%95 Ci | [1.17-1.81] |
Platform | Illumina [307328] |
CNV | N |
Mapped trait | asthma |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000270 |
Study accession | GCST000061 |