Human SNP ID | rs4466998 |
---|---|
Human chromosome | chr14 |
Human SNP position | 65008822 |
Pig chromosome | chr7 |
Pig SNP position | 95460356 |
PubMed ID | 19862010 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/19862010 |
Study | Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. |
Disease/Trait | Mean corpuscular volume |
Initial sample | 24,167 European ancestry individuals |
Replication sample | 9,456 European ancestry individuals |
Region | 14q23.3 |
Chromosome id | chr14 |
Chromosome position | 65008822 |
Reported gene | FNTB |
Mapped gene | FNTB, CHURC1-FNTB, MAX |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 2342, 100529261, 4149 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4466998-A |
SNPs | rs4466998 |
Merged | 0 |
SNP id current | 4466998 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.00000005 |
Pvalue mlog | 7.30102999566398 |
P value text | |
Or beta | 0 |
%95 Ci | [0.001-0.003] fl increase |
Platform | Affymetrix, Illumina [~ 2500000] (imputed) |
CNV | N |
Mapped trait | mean corpuscular volume |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004526 |
Study accession | GCST000503 |