Human SNP ID | rs17556750 |
---|---|
Human chromosome | chr4 |
Human SNP position | 81234414 |
Pig chromosome | chr8 |
Pig SNP position | 146034646 |
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 | 4q21.21 |
Chromosome id | chr4 |
Chromosome position | 81234414 |
Reported gene | PRKG2 |
Mapped gene | PRKG2 - RASGEF1B |
Upstream gene id | 5593 |
Downstream gene id | 153020 |
SNP gene ids | |
Upstream gene distance | 17671 |
Downstream gene distance | 191979 |
SNP risk allele | rs17556750-A |
SNPs | rs17556750 |
Merged | 0 |
SNP id current | 17556750 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.314 |
P value | 8E-48 |
Pvalue mlog | 47.096910013008 |
P value text | |
Or beta | 0.046 |
%95 Ci | [0.04-0.052] 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 |