Human SNP ID | rs2274432 |
---|---|
Human chromosome | chr1 |
Human SNP position | 184051811 |
Pig chromosome | chr9 |
Pig SNP position | 137621761 |
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 | 1q25.3 |
Chromosome id | chr1 |
Chromosome position | 184051811 |
Reported gene | GLT25D2, C1orf19 |
Mapped gene | TSEN15 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 116461 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2274432-T |
SNPs | rs2274432 |
Merged | 0 |
SNP id current | 2274432 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | 0.37 |
P value | 0.000000008 |
Pvalue mlog | 8.09691001300805 |
P value text | |
Or beta | 5.3 |
%95 Ci | [3.54-7.06] % 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 |