Human SNP ID | rs3748069 |
---|---|
Human chromosome | chr6 |
Human SNP position | 142446496 |
Pig chromosome | chr1 |
Pig SNP position | 25213554 |
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 | 6q24.2 |
Chromosome id | chr6 |
Chromosome position | 142446496 |
Reported gene | GPR126 |
Mapped gene | ADGRG6 - LOC153910 |
Upstream gene id | 57211 |
Downstream gene id | 153910 |
SNP gene ids | |
Upstream gene distance | 230 |
Downstream gene distance | 79959 |
SNP risk allele | rs3748069-A |
SNPs | rs3748069 |
Merged | 0 |
SNP id current | 3748069 |
Context | downstream_gene_variant |
Intergenic | 1 |
Allele frequency | 0.74 |
P value | 0.00000000000005 |
Pvalue mlog | 13.3010299956639 |
P value text | |
Or beta | 6.5 |
%95 Ci | [5.44-9.36] % 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 |