Human SNP ID | rs2834442 |
---|---|
Human chromosome | chr21 |
Human SNP position | 34318486 |
Pig chromosome | chr13 |
Pig SNP position | 207757926 |
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 | 21q22.11 |
Chromosome id | chr21 |
Chromosome position | 34318486 |
Reported gene | KCNE2 |
Mapped gene | LINC00310 - LOC105372791 |
Upstream gene id | 114036 |
Downstream gene id | 105372791 |
SNP gene ids | |
Upstream gene distance | 128567 |
Downstream gene distance | 34551 |
SNP risk allele | rs2834442-A |
SNPs | rs2834442 |
Merged | 0 |
SNP id current | 2834442 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | 0.65 |
P value | 0.000000000005 |
Pvalue mlog | 11.3010299956639 |
P value text | |
Or beta | 0.026 |
%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 |