Human SNP ID | rs10514279 |
---|---|
Human chromosome | chr5 |
Human SNP position | 86411652 |
Pig chromosome | chr2 |
Pig SNP position | 96728111 |
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 | 5q14.3 x 6q25.1 |
Chromosome id | chr5 x 6 |
Chromosome position | 86411652 x 151152195 |
Reported gene | NR x NR |
Mapped gene | LOC105379064 x LOC105378057 - LOC102723831 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10514279-? x rs4869993-? |
SNPs | rs10514279 x rs4869993 |
Merged | |
SNP id current | |
Context | intergenic_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 |