Human SNP ID | rs2287623 |
---|---|
Human chromosome | chr2 |
Human SNP position | 168973645 |
Pig chromosome | chr15 |
Pig SNP position | 84549555 |
PubMed ID | 24097068 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/24097068 |
Study | Discovery and refinement of loci associated with lipid levels. |
Disease/Trait | Cholesterol, total |
Initial sample | 94,595 European ancestry individuals |
Replication sample | 93,982 European ancestry individuals |
Region | 2q31.1 |
Chromosome id | chr2 |
Chromosome position | 168973645 |
Reported gene | ABCB11 |
Mapped gene | ABCB11 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 8647 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2287623-G |
SNPs | rs2287623 |
Merged | 0 |
SNP id current | 2287623 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.41 |
P value | 0.000000000004 |
Pvalue mlog | 11.397940008672 |
P value text | |
Or beta | 0.027 |
%95 Ci | [NR] unit increase |
Platform | NR [NR] (imputed) |
CNV | N |
Mapped trait | total cholesterol measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004574 |
Study accession | GCST002221 |