Human SNP ID | rs8007661 |
---|---|
Human chromosome | chr14 |
Human SNP position | 91993614 |
Pig chromosome | chr7 |
Pig SNP position | 120157080 |
PubMed ID | 18391950 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/18391950 |
Study | Identification of ten loci associated with height highlights new biological pathways in human growth. |
Disease/Trait | Height |
Initial sample | 15,821 European ancestry individuals |
Replication sample | Up to 17,801 European ancestry individuals |
Region | 14q32.12 |
Chromosome id | chr14 |
Chromosome position | 91993614 |
Reported gene | TRIP11, ATXN3 |
Mapped gene | TRIP11 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 9321 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs8007661-T |
SNPs | rs8007661 |
Merged | 0 |
SNP id current | 8007661 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.3 |
P value | 0.0000000006 |
Pvalue mlog | 9.22184874961635 |
P value text | |
Or beta | 0.42 |
%95 Ci | [0.30-0.54] cm decrease |
Platform | Affymetrix, Illumina [2260683] (imputed) |
CNV | N |
Mapped trait | body height |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004339 |
Study accession | GCST000176 |