Human SNP ID | rs116864947 |
---|---|
Human chromosome | chr7 |
Human SNP position | 11666159 |
Pig chromosome | chr9 |
Pig SNP position | 89335273 |
PubMed ID | 25820613 |
---|---|
Journal | Hum Mol Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/25820613 |
Study | Genome-wide association study of blood lead shows multiple associations near ALAD. |
Disease/Trait | Lead levels in blood |
Initial sample | 5,433 individuals |
Replication sample | NA |
Region | 7p21.3 |
Chromosome id | chr7 |
Chromosome position | 11666159 |
Reported gene | THSD7A |
Mapped gene | THSD7A |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 221981 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs116864947-T |
SNPs | rs116864947 |
Merged | 0 |
SNP id current | 116864947 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.983 |
P value | 0.0000003 |
Pvalue mlog | 6.52287874528033 |
P value text | |
Or beta | 0.431 |
%95 Ci | [0.23-0.63] unit decrease |
Platform | Illumina [6391392] (imputed) |
CNV | N |
Mapped trait | blood lead measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0007040 |
Study accession | GCST002831 |