Human SNP ID | rs2638953 |
---|---|
Human chromosome | chr12 |
Human SNP position | 28381482 |
Pig chromosome | chr5 |
Pig SNP position | 48679425 |
PubMed ID | 20881960 |
---|---|
Journal | Nature |
Link | www.ncbi.nlm.nih.gov/pubmed/20881960 |
Study | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
Disease/Trait | Height |
Initial sample | 133,653 European ancestry individuals |
Replication sample | 50,074 European ancestry individuals |
Region | 12p11.22 |
Chromosome id | chr12 |
Chromosome position | 28381482 |
Reported gene | CCDC91 |
Mapped gene | CCDC91 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 55297 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2638953-C |
SNPs | rs2638953 |
Merged | 0 |
SNP id current | 2638953 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.68 |
P value | 0.00000000000000007 |
Pvalue mlog | 16.1549019599857 |
P value text | |
Or beta | 0.032 |
%95 Ci | [NR] unit increase |
Platform | Affymetrix, Illumina [2834208] (imputed) |
CNV | N |
Mapped trait | body height |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004339 |
Study accession | GCST000817 |