Human SNP ID | rs877549 |
---|---|
Human chromosome | chr22 |
Human SNP position | 30276431 |
Pig chromosome | chr14 |
Pig SNP position | 50294289 |
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 | 4p16.2 x 22q12.2 |
Chromosome id | chr4 x 22 |
Chromosome position | 4652630 x 30276431 |
Reported gene | NR x NR |
Mapped gene | STX18-AS1 x OSM - GATSL3 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2063413-? x rs877549-? |
SNPs | rs2063413 x rs877549 |
Merged | |
SNP id current | |
Context | intron_variant x non_coding_transcript_exon_variant |
Intergenic | |
Allele frequency | NR |
P value | 0.000000005 |
Pvalue mlog | 8.30102999566398 |
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 |