Human SNP ID | rs6904029 |
---|---|
Human chromosome | chr6 |
Human SNP position | 29975290 |
Pig chromosome | chr7 |
Pig SNP position | 27233320 |
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 | 6p22.1 |
Chromosome id | chr6 |
Chromosome position | 29975290 |
Reported gene | HLA-A29.1, HCG9 |
Mapped gene | HCG9 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 10255 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs6904029-? |
SNPs | rs6904029 |
Merged | 0 |
SNP id current | 6904029 |
Context | non_coding_transcript_exon_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | (PC3) |
Or beta | 0.0464 |
%95 Ci | [NR] unit decrease |
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 |