Human SNP ID | rs1814175 |
---|---|
Human chromosome | chr11 |
Human SNP position | 49537620 |
Pig chromosome | chr9 |
Pig SNP position | 25103966 |
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 | 11p11.12 |
Chromosome id | chr11 |
Chromosome position | 49537620 |
Reported gene | FOLH1 |
Mapped gene | LOC653698 - LOC105376665 |
Upstream gene id | 653698 |
Downstream gene id | 105376665 |
SNP gene ids | |
Upstream gene distance | 102958 |
Downstream gene distance | 16742 |
SNP risk allele | rs1814175-T |
SNPs | rs1814175 |
Merged | 0 |
SNP id current | 1814175 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.34 |
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 |