Human SNP ID | rs1401796 |
---|---|
Human chromosome | chr17 |
Human SNP position | 56762398 |
Pig chromosome | chr12 |
Pig SNP position | 33894873 |
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 | 17q22 |
Chromosome id | chr17 |
Chromosome position | 56762398 |
Reported gene | NOG |
Mapped gene | NOG - C17orf67 |
Upstream gene id | 9241 |
Downstream gene id | 339210 |
SNP gene ids | |
Upstream gene distance | 166808 |
Downstream gene distance | 29515 |
SNP risk allele | rs1401796-? |
SNPs | rs1401796 |
Merged | 0 |
SNP id current | 1401796 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.00000002 |
Pvalue mlog | 7.69897000433601 |
P value text | (Conditioned on rs227724) |
Or beta | |
%95 Ci | [NR] |
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 |