Human SNP ID | rs7710527 |
---|---|
Human chromosome | chr5 |
Human SNP position | 109166792 |
Pig chromosome | chr2 |
Pig SNP position | 118673003 |
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 | 5q21.3 x 7p14.1 |
Chromosome id | chr5 x 7 |
Chromosome position | 109166792 x 42324206 |
Reported gene | NR x NR |
Mapped gene | FER, LOC105379115 x GLI3 - LOC105375249 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7710527-? x rs10278194-? |
SNPs | rs7710527 x rs10278194 |
Merged | |
SNP id current | |
Context | intron_variant x intergenic_variant |
Intergenic | |
Allele frequency | NR |
P value | 0.000000006 |
Pvalue mlog | 8.22184874961635 |
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 |