Human SNP ID | rs7864648 |
---|---|
Human chromosome | chr9 |
Human SNP position | 16368734 |
Pig chromosome | chr1 |
Pig SNP position | 230165553 |
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 | 9p22.3 |
Chromosome id | chr9 |
Chromosome position | 16368734 |
Reported gene | BNC2 |
Mapped gene | C9orf92 - BNC2 |
Upstream gene id | 100129385 |
Downstream gene id | 54796 |
SNP gene ids | |
Upstream gene distance | 92421 |
Downstream gene distance | 40769 |
SNP risk allele | rs7864648-T |
SNPs | rs7864648 |
Merged | 0 |
SNP id current | 7864648 |
Context | regulatory_region_variant |
Intergenic | 1 |
Allele frequency | 0.32 |
P value | 0.00000002 |
Pvalue mlog | 7.69897000433601 |
P value text | |
Or beta | 0.022 |
%95 Ci | [NR] unit increase |
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 |