Human SNP ID | rs2162234 |
---|---|
Human chromosome | chr15 |
Human SNP position | 83713683 |
Pig chromosome | chr7 |
Pig SNP position | 56688824 |
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 | 7q32.2 x 15q25.2 |
Chromosome id | chr7 x 15 |
Chromosome position | 130363646 x 83713683 |
Reported gene | NR x NR |
Mapped gene | CPA5 x ADAMTSL3 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs17164851-? x rs2162234-? |
SNPs | rs17164851 x rs2162234 |
Merged | |
SNP id current | |
Context | intron_variant x intron_variant |
Intergenic | |
Allele frequency | NR |
P value | 0.000000002 |
Pvalue mlog | 8.69897000433601 |
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 |