Human SNP ID | rs563748 |
---|---|
Human chromosome | chr11 |
Human SNP position | 59999026 |
Pig chromosome | chr2 |
Pig SNP position | 10999235 |
PubMed ID | 24939585 |
---|---|
Journal | Eur J Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/24939585 |
Study | Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. |
Disease/Trait | Age-related hearing impairment (interaction) |
Initial sample | 1,489 European ancestry individuals |
Replication sample | NA |
Region | 10q24.2 x 11q12.1 |
Chromosome id | chr10 x 11 |
Chromosome position | 100063786 x 59999026 |
Reported gene | NR x NR |
Mapped gene | CPN1 x OOSP1 - LOC105369444 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4462272-? x rs563748-? |
SNPs | rs4462272 x rs563748 |
Merged | |
SNP id current | |
Context | intron_variant x downstream_gene_variant |
Intergenic | |
Allele frequency | NR |
P value | 0.000000008 |
Pvalue mlog | 8.09691001300805 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [629437] (imputed) |
CNV | N |
Mapped trait | age-related hearing impairment |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005782 |
Study accession | GCST002487 |