Human SNP ID | rs12346772 |
---|---|
Human chromosome | chr9 |
Human SNP position | 111158319 |
Pig chromosome | chr1 |
Pig SNP position | 282901176 |
PubMed ID | 25096241 |
---|---|
Journal | Hum Mol Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25096241 |
Study | Trans-ethnic meta-analysis of white blood cell phenotypes. |
Disease/Trait | Monocyte count |
Initial sample | 9,810 Japanese ancestry individuals, 16,550 European ancestry individuals, 7,369 African American individuals |
Replication sample | NA |
Region | 9q31.3 |
Chromosome id | chr9 |
Chromosome position | 111158319 |
Reported gene | NR |
Mapped gene | LOC105376219 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105376219 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs12346772-? |
SNPs | rs12346772 |
Merged | 0 |
SNP id current | 12346772 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.0000000001 |
Pvalue mlog | 10 |
P value text | |
Or beta | 0.0226 |
%95 Ci | [0.016-0.029] unit decrease |
Platform | Illumina [NR] (imputed) |
CNV | N |
Mapped trait | monocyte count |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005091 |
Study accession | GCST002555 |