Human SNP ID | rs2445284 |
---|---|
Human chromosome | chr11 |
Human SNP position | 5008473 |
Pig chromosome | chr9 |
Pig SNP position | 5811243 |
PubMed ID | 23406172 |
---|---|
Journal | Br J Haematol |
Link | www.ncbi.nlm.nih.gov/pubmed/23406172 |
Study | Genetic determinants of haemolysis in sickle cell anaemia. |
Disease/Trait | Sickle cell anemia (haemolysis) |
Initial sample | 1,117 individuals |
Replication sample | 213 African ancestry, West African ancestry and Afro-Caribbean individuals, 745 individuals |
Region | 11p15.4 |
Chromosome id | chr11 |
Chromosome position | 5008473 |
Reported gene | OR51L1 |
Mapped gene | OR51L1 - OR52J3 |
Upstream gene id | 119682 |
Downstream gene id | 119679 |
SNP gene ids | |
Upstream gene distance | 8543 |
Downstream gene distance | 38053 |
SNP risk allele | rs2445284-G |
SNPs | rs2445284 |
Merged | 0 |
SNP id current | 2445284 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.05 |
P value | 1E-29 |
Pvalue mlog | 29 |
P value text | |
Or beta | 0.82 |
%95 Ci | [0.68-0.96] unit decrease |
Platform | Illumina [569554] |
CNV | N |
Mapped trait | Sickle cell anemia |
Mapped trait URI | http://www.orpha.net/ORDO/Orphanet_232 |
Study accession | GCST001862 |