Human SNP ID | rs737092 |
---|---|
Human chromosome | chr20 |
Human SNP position | 57415349 |
Pig chromosome | chr17 |
Pig SNP position | 64969042 |
PubMed ID | 23222517 |
---|---|
Journal | Nature |
Link | www.ncbi.nlm.nih.gov/pubmed/23222517 |
Study | Seventy-five genetic loci influencing the human red blood cell. |
Disease/Trait | Red blood cell traits |
Initial sample | 62,553 European ancestry individuals, 9,308 South Asian ancestry individuals |
Replication sample | 63,506 European ancestry individuals |
Region | 20q13.31 |
Chromosome id | chr20 |
Chromosome position | 57415349 |
Reported gene | RBM38 |
Mapped gene | RBM38 - LOC105372688 |
Upstream gene id | 55544 |
Downstream gene id | 105372688 |
SNP gene ids | |
Upstream gene distance | 6016 |
Downstream gene distance | 45125 |
SNP risk allele | rs737092-C |
SNPs | rs737092 |
Merged | 0 |
SNP id current | 737092 |
Context | regulatory_region_variant |
Intergenic | 1 |
Allele frequency | 0.49 |
P value | 0.0000000000004 |
Pvalue mlog | 12.397940008672 |
P value text | (EA, MCV) |
Or beta | 0.216 |
%95 Ci | [0.15-0.28] unit increase |
Platform | Affymetrix, Illumina, Perlegen [2711806] (imputed) |
CNV | N |
Mapped trait | mean corpuscular volume |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004526 |
Study accession | GCST001765 |