Human SNP ID | rs1239947 |
---|---|
Human chromosome | chr13 |
Human SNP position | 50532419 |
Pig chromosome | chr11 |
Pig SNP position | 17555104 |
PubMed ID | 18391951 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/18391951 |
Study | Many sequence variants affecting diversity of adult human height. |
Disease/Trait | Height |
Initial sample | 30,968 European ancestry individuals |
Replication sample | 8,541 European ancestry individuals |
Region | 13q14.3 |
Chromosome id | chr13 |
Chromosome position | 50532419 |
Reported gene | DLEU7 |
Mapped gene | DLEU1 - DLEU7 |
Upstream gene id | 10301 |
Downstream gene id | 220107 |
SNP gene ids | |
Upstream gene distance | 3776 |
Downstream gene distance | 163131 |
SNP risk allele | rs1239947-G |
SNPs | rs1239947 |
Merged | 0 |
SNP id current | 1239947 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | 0.35 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | |
Or beta | 3.8 |
%95 Ci | [2.23-5.37] % s.d. increase |
Platform | Affymetrix, Illumina [up to 304226] |
CNV | N |
Mapped trait | body height |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004339 |
Study accession | GCST000175 |