Human SNP ID | rs10859567 |
---|---|
Human chromosome | chr12 |
Human SNP position | 93733149 |
Pig chromosome | chr5 |
Pig SNP position | 93874851 |
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 | 12q22 |
Chromosome id | chr12 |
Chromosome position | 93733149 |
Reported gene | CRADD |
Mapped gene | LOC101928731, CRADD |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 101928731, 8738 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10859567-T |
SNPs | rs10859567 |
Merged | 0 |
SNP id current | 10859567 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.563 |
P value | 5E-33 |
Pvalue mlog | 32.3010299956639 |
P value text | |
Or beta | 0.035 |
%95 Ci | [0.029-0.041] 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 |