Human SNP ID | rs1367226 |
---|---|
Human chromosome | chr2 |
Human SNP position | 55862405 |
Pig chromosome | chr3 |
Pig SNP position | 90201071 |
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 | 2p16.1 |
Chromosome id | chr2 |
Chromosome position | 55862405 |
Reported gene | EFEMP1 |
Mapped gene | LOC105374679 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105374679 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1367226-? |
SNPs | rs1367226 |
Merged | 0 |
SNP id current | 1367226 |
Context | downstream_gene_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.00000004 |
Pvalue mlog | 7.39794000867203 |
P value text | (Conditioned on rs3791675) |
Or beta | |
%95 Ci | [NR] |
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 |