Human SNP ID | rs7594648 |
---|---|
Human chromosome | chr2 |
Human SNP position | 155679341 |
Pig chromosome | chr15 |
Pig SNP position | 70179346 |
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 |
Initial sample | 1,489 European ancestry individuals |
Replication sample | NA |
Region | 2q24.1 |
Chromosome id | chr2 |
Chromosome position | 155679341 |
Reported gene | intergenic |
Mapped gene | LOC105373700 - LOC105373701 |
Upstream gene id | 105373700 |
Downstream gene id | 105373701 |
SNP gene ids | |
Upstream gene distance | 190003 |
Downstream gene distance | 80305 |
SNP risk allele | rs7594648-? |
SNPs | rs7594648 |
Merged | 0 |
SNP id current | 7594648 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
P value text | (PC3) |
Or beta | 0.0443 |
%95 Ci | [NR] unit increase |
Platform | Illumina [4167292] (imputed) |
CNV | N |
Mapped trait | age-related hearing impairment |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005782 |
Study accession | GCST002491 |