Human SNP ID | rs12209223 |
---|---|
Human chromosome | chr6 |
Human SNP position | 75454873 |
Pig chromosome | chr1 |
Pig SNP position | 101505492 |
PubMed ID | 25282103 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25282103 |
Study | Defining the role of common variation in the genomic and biological architecture of adult human height. |
Disease/Trait | Height |
Initial sample | 253,288 European ancestry individuals |
Replication sample | 80,067 European ancestry individuals |
Region | 6q14.1 |
Chromosome id | chr6 |
Chromosome position | 75454873 |
Reported gene | FILIP1 |
Mapped gene | LOC101928540, FILIP1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 101928540, 27145 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs12209223-A |
SNPs | rs12209223 |
Merged | 0 |
SNP id current | 12209223 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.116 |
P value | 5E-25 |
Pvalue mlog | 24.3010299956639 |
P value text | |
Or beta | 0.051 |
%95 Ci | [0.041-0.061] unit increase |
Platform | Affymetrix, Illumina, Perlegen [2550858] (imputed) |
CNV | N |
Mapped trait | body height |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004339 |
Study accession | GCST002647 |