Human SNP ID | rs10445033 |
---|---|
Human chromosome | chr16 |
Human SNP position | 88774054 |
Pig chromosome | chr6 |
Pig SNP position | 1109606 |
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 | 16q24.3 |
Chromosome id | chr16 |
Chromosome position | 88774054 |
Reported gene | FAM38A, PIEZO1 |
Mapped gene | PIEZO1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 9780 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10445033-G |
SNPs | rs10445033 |
Merged | 0 |
SNP id current | 10445033 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.37 |
P value | 2E-22 |
Pvalue mlog | 21.698970004336 |
P value text | (EA, MCHC) |
Or beta | 0.02 |
%95 Ci | [-0.00352-0.04352] unit increase |
Platform | Affymetrix, Illumina, Perlegen [2711806] (imputed) |
CNV | N |
Mapped trait | mean corpuscular hemoglobin concentration |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004528 |
Study accession | GCST001765 |