Human SNP ID | rs318095 |
---|---|
Human chromosome | chr17 |
Human SNP position | 48897372 |
Pig chromosome | chr12 |
Pig SNP position | 25070279 |
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 | 17q21.32 |
Chromosome id | chr17 |
Chromosome position | 48897372 |
Reported gene | ATP5G1 |
Mapped gene | ATP5G1 - UBE2Z |
Upstream gene id | 516 |
Downstream gene id | 65264 |
SNP gene ids | |
Upstream gene distance | 1501 |
Downstream gene distance | 10997 |
SNP risk allele | rs318095-T |
SNPs | rs318095 |
Merged | 0 |
SNP id current | 318095 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | 0.463 |
P value | 0.0000000000000002 |
Pvalue mlog | 15.698970004336 |
P value text | |
Or beta | 0.024 |
%95 Ci | [0.018-0.03] 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 |