Human SNP ID | rs17170356 |
---|---|
Human chromosome | chr7 |
Human SNP position | 147190776 |
Pig chromosome | chr9 |
Pig SNP position | 121875824 |
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 | 7q35 |
Chromosome id | chr7 |
Chromosome position | 147190776 |
Reported gene | CNTNAP2 |
Mapped gene | CNTNAP2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 26047 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs17170356-? |
SNPs | rs17170356 |
Merged | 0 |
SNP id current | 17170356 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | (PC3) |
Or beta | 0.1547 |
%95 Ci | [NR] unit increase |
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 |