Human SNP ID | rs822531 |
---|---|
Human chromosome | chr7 |
Human SNP position | 148932667 |
Pig chromosome | chr9 |
Pig SNP position | 120270304 |
PubMed ID | 25282103 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25282103 |
Study | Defining the role of common variation in the genomic and biological architecture of adult human height. |
Disease/Trait | Height |
Initial sample | 253,288 European ancestry individuals |
Replication sample | 80,067 European ancestry individuals |
Region | 7q36.1 |
Chromosome id | chr7 |
Chromosome position | 148932667 |
Reported gene | EZH2 |
Mapped gene | EZH2 - RNY5 |
Upstream gene id | 2146 |
Downstream gene id | 6090 |
SNP gene ids | |
Upstream gene distance | 48318 |
Downstream gene distance | 8821 |
SNP risk allele | rs822531-T |
SNPs | rs822531 |
Merged | 0 |
SNP id current | 822531 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.776 |
P value | 0.000000000000000002 |
Pvalue mlog | 17.698970004336 |
P value text | |
Or beta | 0.036 |
%95 Ci | [0.028-0.044] unit increase |
Platform | Affymetrix, Illumina, Perlegen [2550858] (imputed) |
CNV | N |
Mapped trait | body height |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004339 |
Study accession | GCST002647 |