Human SNP ID | rs2430212 |
---|---|
Human chromosome | chrX |
Human SNP position | 117954093 |
Pig chromosome | chrX |
Pig SNP position | 114963594 |
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 | Xq24 |
Chromosome id | chrX |
Chromosome position | 117954093 |
Reported gene | KLHL13 |
Mapped gene | KLHL13 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 90293 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2430212-? |
SNPs | rs2430212 |
Merged | 0 |
SNP id current | 2430212 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | (serum transferrin) |
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 |