Human SNP ID | rs11259936 |
---|---|
Human chromosome | chr15 |
Human SNP position | 83911830 |
Pig chromosome | chr7 |
Pig SNP position | 56623183 |
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 | 15q25.2 |
Chromosome id | chr15 |
Chromosome position | 83911830 |
Reported gene | ADAMTSL3 |
Mapped gene | ADAMTSL3 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 57188 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11259936-A |
SNPs | rs11259936 |
Merged | 0 |
SNP id current | 11259936 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.48 |
P value | 2E-35 |
Pvalue mlog | 34.698970004336 |
P value text | |
Or beta | 0.044 |
%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 |