Human SNP ID | rs9844666 |
---|---|
Human chromosome | chr3 |
Human SNP position | 136255374 |
Pig chromosome | chr13 |
Pig SNP position | 84590930 |
PubMed ID | 20881960 |
---|---|
Journal | Nature |
Link | www.ncbi.nlm.nih.gov/pubmed/20881960 |
Study | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Disease/Trait | Height |
Initial sample | 133,653 European ancestry individuals |
Replication sample | 50,074 European ancestry individuals |
Region | 3q22.3 |
Chromosome id | chr3 |
Chromosome position | 136255374 |
Reported gene | PCCB |
Mapped gene | PCCB |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 5096 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs9844666-A |
SNPs | rs9844666 |
Merged | 0 |
SNP id current | 9844666 |
Context | 5_prime_UTR_variant |
Intergenic | 0 |
Allele frequency | 0.25 |
P value | 0.000000004 |
Pvalue mlog | 8.39794000867203 |
P value text | |
Or beta | 0.024 |
%95 Ci | [NR] unit decrease |
Platform | Affymetrix, Illumina [2834208] (imputed) |
CNV | N |
Mapped trait | body height |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004339 |
Study accession | GCST000817 |