Human SNP ID | rs10444487 |
---|---|
Human chromosome | chr12 |
Human SNP position | 116163253 |
Pig chromosome | chr14 |
Pig SNP position | 38379205 |
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 | 6p21.1 x 12q24.21 |
Chromosome id | chr6 x 12 |
Chromosome position | 40635318 x 116163253 |
Reported gene | NR x NR |
Mapped gene | LRFN2 - LOC101929535 x MED13L |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4301303-? x rs10444487-? |
SNPs | rs4301303 x rs10444487 |
Merged | |
SNP id current | |
Context | intergenic_variant x intron_variant |
Intergenic | |
Allele frequency | NR |
P value | 0.000000007 |
Pvalue mlog | 8.15490195998574 |
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 |