Human SNP ID | rs12651106 |
---|---|
Human chromosome | chr4 |
Human SNP position | 154379907 |
Pig chromosome | chr8 |
Pig SNP position | 79276684 |
PubMed ID | 21757653 |
---|---|
Journal | Arterioscler Thromb Vasc Biol |
Link | www.ncbi.nlm.nih.gov/pubmed/21757653 |
Study | Assessment of genetic determinants of the association of γ__ fibrinogen in relation to cardiovascular disease. |
Disease/Trait | Fibrinogen |
Initial sample | 3,042 individuals |
Replication sample | NA |
Region | 4q31.3 |
Chromosome id | chr4 |
Chromosome position | 154379907 |
Reported gene | DCHS2 |
Mapped gene | DCHS2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 54798 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs12651106-A |
SNPs | rs12651106 |
Merged | 0 |
SNP id current | 12651106 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.17 |
P value | 0.000000000002 |
Pvalue mlog | 11.698970004336 |
P value text | |
Or beta | 0.14 |
%95 Ci | [0.10-0.18] g/L decrease |
Platform | Affymetrix [~ 2500000] (imputed) |
CNV | N |
Mapped trait | fibrinogen measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004623 |
Study accession | GCST001158 |