Human SNP ID | rs11775334 |
---|---|
Human chromosome | chr8 |
Human SNP position | 10214110 |
Pig chromosome | chr14 |
Pig SNP position | 14839154 |
PubMed ID | 19430479 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/19430479 |
Study | Genome-wide association study of blood pressure and hypertension. |
Disease/Trait | Hypertension |
Initial sample | 29,136 European ancestry individuals |
Replication sample | 34,433 European ancestry individuals |
Region | 8p23.1 |
Chromosome id | chr8 |
Chromosome position | 10214110 |
Reported gene | MSRA |
Mapped gene | MSRA |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 4482 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11775334-A |
SNPs | rs11775334 |
Merged | 0 |
SNP id current | 11775334 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.32 |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | |
Or beta | 0.08 |
%95 Ci | [0.04-0.12] log odds increase |
Platform | Affymetrix, Illumina [2533153] (imputed) |
CNV | N |
Mapped trait | hypertension |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000537 |
Study accession | GCST000398 |