Human SNP ID | rs1712790 |
---|---|
Human chromosome | chr11 |
Human SNP position | 114750747 |
Pig chromosome | chr9 |
Pig SNP position | 47028916 |
PubMed ID | 17903292 |
---|---|
Journal | BMC Med Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/17903292 |
Study | A genome-wide association for kidney function and endocrine-related traits in the NHLBI__s Framingham Heart Study. |
Disease/Trait | Urinary albumin excretion |
Initial sample | 822 individuals |
Replication sample | NA |
Region | 11q23.3 |
Chromosome id | chr11 |
Chromosome position | 114750747 |
Reported gene | FAM55B |
Mapped gene | NXPE2 - LOC105369506 |
Upstream gene id | 120406 |
Downstream gene id | 105369506 |
SNP gene ids | |
Upstream gene distance | 43630 |
Downstream gene distance | 28924 |
SNP risk allele | rs1712790-? |
SNPs | rs1712790 |
Merged | 0 |
SNP id current | 1712790 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Affymetrix [70897] |
CNV | N |
Mapped trait | albuminuria |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004285 |
Study accession | GCST000105 |