Human SNP ID | 6x121088770-? |
---|---|
Human chromosome | chr9 |
Human SNP position | 34646737 |
Pig chromosome | chr10 |
Pig SNP position | 36294526 |
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 | 9p13.3 |
Chromosome id | chr9 |
Chromosome position | 34646737 |
Reported gene | intergenic x intergenic |
Mapped gene | GALT x No mapped genes |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | 6 x 121088770 |
SNPs | 6 x 121088770-? |
Merged | |
SNP id current | |
Context | synonymous_variant |
Intergenic | |
Allele frequency | |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (PC1) |
Or beta | 0.3022 |
%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 |