Human SNP ID | rs931726 |
---|---|
Human chromosome | chr3 |
Human SNP position | 135212098 |
Pig chromosome | chr13 |
Pig SNP position | 83824647 |
PubMed ID | 25865494 |
---|---|
Journal | Am J Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25865494 |
Study | Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development. |
Disease/Trait | Sitting height ratio |
Initial sample | 3,545 African Americans individuals, 12,965 European ancestry women, 8,625 European ancestry men |
Replication sample | NA |
Region | 3q22.2 |
Chromosome id | chr3 |
Chromosome position | 135212098 |
Reported gene | NR |
Mapped gene | EPHB1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 2047 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs931726-T |
SNPs | rs931726 |
Merged | 0 |
SNP id current | 931726 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.25 |
P value | 0.0000006 |
Pvalue mlog | 6.22184874961635 |
P value text | (EA) |
Or beta | 0.056 |
%95 Ci | [0.034-0.078] unit increase |
Platform | Affymetrix, Illumina [up to 10250422] (imputed) |
CNV | N |
Mapped trait | sitting height ratio |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0007118 |
Study accession | GCST002843 |