Human SNP ID | rs2255811 |
---|---|
Human chromosome | chr7 |
Human SNP position | 113082141 |
Pig chromosome | chr18 |
Pig SNP position | 35228027 |
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 | Triglycerides |
Initial sample | up to 62,166 European ancestry individuals |
Replication sample | NA |
Region | 7q31.1 |
Chromosome id | chr7 |
Chromosome position | 113082141 |
Reported gene | GPR85 |
Mapped gene | GPR85 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 54329 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2255811-G |
SNPs | rs2255811 |
Merged | |
SNP id current | 2255811 |
Context | 3_prime_UTR_variant |
Intergenic | 0 |
Allele frequency | 0.25 |
P value | 0.00000002 |
Pvalue mlog | 7.69897000433601 |
P value text | |
Or beta | 0.041 |
%95 Ci | [0.027-0.055] s.d. increase |
Platform | Affymetrix, Illumina, Perlegen [up to 9657952] (imputed) |
CNV | N |
Mapped trait | triglyceride measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004530 |
Study accession | GCST002897 |