Human SNP ID | rs13241165 |
---|---|
Human chromosome | chr7 |
Human SNP position | 130747779 |
Pig chromosome | chr18 |
Pig SNP position | 19154480 |
PubMed ID | 25961943 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25961943 |
Study | The impact of low-frequency and rare variants on lipid levels. |
Disease/Trait | HDL cholesterol |
Initial sample | up to 62,166 European ancestry individuals |
Replication sample | NA |
Region | 7q32.2 |
Chromosome id | chr7 |
Chromosome position | 130747779 |
Reported gene | KLF14 |
Mapped gene | LOC105375508 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105375508 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs13241165-T |
SNPs | rs13241165 |
Merged | |
SNP id current | 13241165 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | 0.51 |
P value | 0.0000000008 |
Pvalue mlog | 9.09691001300805 |
P value text | |
Or beta | 0.037 |
%95 Ci | [0.025-0.049] s.d. increase |
Platform | Affymetrix, Illumina, Perlegen [up to 9657952] (imputed) |
CNV | N |
Mapped trait | high density lipoprotein cholesterol measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004612 |
Study accession | GCST002899 |
PubMed ID | 25961943 |
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25961943 |
Study | The impact of low-frequency and rare variants on lipid levels. |
Disease/Trait | HDL cholesterol |
Initial sample | up to 62,166 European ancestry individuals |
Replication sample | NA |
Region | 7q32.2 |
Chromosome id | chr7 |
Chromosome position | 130747779 |
Reported gene | KLF14 |
Mapped gene | LOC105375508 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105375508 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs13241165-T |
SNPs | rs13241165 |
Merged | |
SNP id current | 13241165 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | 0.51 |
P value | 0.0000000008 |
Pvalue mlog | 9.09691001300805 |
P value text | |
Or beta | 0.037 |
%95 Ci | [0.025-0.049] s.d. increase |
Platform | Affymetrix, Illumina, Perlegen [up to 9657952] (imputed) |
CNV | N |
Mapped trait | high density lipoprotein cholesterol measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004612 |
Study accession | GCST002899 |