Human SNP ID | rs13068223 |
---|---|
Human chromosome | chr3 |
Human SNP position | 156753166 |
Pig chromosome | chr13 |
Pig SNP position | 104684611 |
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 | 3q25.31 x 11p15.3 |
Chromosome id | chr3 x 11 |
Chromosome position | 156753166 x 12434135 |
Reported gene | NR x NR |
Mapped gene | LINC00886 x PARVA |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs13068223-? x rs884272-? |
SNPs | rs13068223 x rs884272 |
Merged | |
SNP id current | |
Context | non_coding_transcript_exon_variant x intron_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 |