Human SNP ID | rs11126435 |
---|---|
Human chromosome | chr2 |
Human SNP position | 74562573 |
Pig chromosome | chr3 |
Pig SNP position | 71663078 |
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 | 2p13.1 x 9p22.2 |
Chromosome id | chr2 x 9 |
Chromosome position | 74562573 x 17009483 |
Reported gene | NR x NR |
Mapped gene | M1AP x BNC2 - LOC105375983 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11126435-? x rs263655-? |
SNPs | rs11126435 x rs263655 |
Merged | |
SNP id current | |
Context | intron_variant x intergenic_variant |
Intergenic | |
Allele frequency | NR |
P value | 0.000000009 |
Pvalue mlog | 8.04575749056067 |
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 |