Human SNP ID | rs447921 |
---|---|
Human chromosome | chr17 |
Human SNP position | 76418477 |
Pig chromosome | chr12 |
Pig SNP position | 4992893 |
PubMed ID | 25240745 |
---|---|
Journal | Mitochondrion |
Link | www.ncbi.nlm.nih.gov/pubmed/25240745 |
Study | A genome-wide association study in the genetic analysis of idiopathic thrombophilia project suggests sex-specific regulation of mitochondrial DNA levels. |
Disease/Trait | Mitochondrial DNA levels |
Initial sample | 173 European ancestry males and 213 European ancestry females from 21 families |
Replication sample | NA |
Region | 17q25.1 |
Chromosome id | chr17 |
Chromosome position | 76418477 |
Reported gene | UBE2O |
Mapped gene | UBE2O |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 63893 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs447921-? |
SNPs | rs447921 |
Merged | 0 |
SNP id current | 447921 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000009 |
Pvalue mlog | 5.04575749056067 |
P value text | |
Or beta | |
%95 Ci | [NR] |
Platform | Illumina [283437] |
CNV | N |
Mapped trait | mitochondrial DNA measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006312 |
Study accession | GCST002616 |