Human SNP ID | rs2660917 |
---|---|
Human chromosome | chr18 |
Human SNP position | 70960842 |
Pig chromosome | chr1 |
Pig SNP position | 168346215 |
PubMed ID | 19084217 |
---|---|
Journal | Am J Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/19084217 |
Study | Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. |
Disease/Trait | Iron status biomarkers |
Initial sample | 459 European ancestry twin pairs |
Replication sample | NA |
Region | 18q22.2 |
Chromosome id | chr18 |
Chromosome position | 70960842 |
Reported gene | intergenic |
Mapped gene | LOC105372185 - LOC105372188 |
Upstream gene id | 105372185 |
Downstream gene id | 105372188 |
SNP gene ids | |
Upstream gene distance | 174089 |
Downstream gene distance | 237116 |
SNP risk allele | rs2660917-? |
SNPs | rs2660917 |
Merged | 0 |
SNP id current | 2660917 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (serum ferritin) |
Or beta | |
%95 Ci | |
Platform | Illumina [315887] |
CNV | N |
Mapped trait | iron biomarker measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004461 |
Study accession | GCST000301 |