Human SNP ID | rs877674 |
---|---|
Human chromosome | chr1 |
Human SNP position | 31776605 |
Pig chromosome | chr6 |
Pig SNP position | 81937853 |
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 | 1p35.2 x 7q21.3 |
Chromosome id | chr1 x 7 |
Chromosome position | 31776605 x 95917441 |
Reported gene | NR x NR |
Mapped gene | ADGRB2 - SPOCD1 x DYNC1I1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs877674-? x rs6952893-? |
SNPs | rs877674 x rs6952893 |
Merged | |
SNP id current | |
Context | intergenic_variant x intron_variant |
Intergenic | |
Allele frequency | NR |
P value | 0.00000000004 |
Pvalue mlog | 10.397940008672 |
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 |