Human SNP ID | rs17440619 |
---|---|
Human chromosome | chr1 |
Human SNP position | 106887973 |
Pig chromosome | chr4 |
Pig SNP position | 123628239 |
PubMed ID | 26116289 |
---|---|
Journal | Exp Gerontol |
Link | www.ncbi.nlm.nih.gov/pubmed/26116289 |
Study | Genetic determinants of swallowing impairments among community dwelling older population. |
Disease/Trait | Dysphagia |
Initial sample | 71 European ancestry older adult cases, 484 European ancestry older adult controls |
Replication sample | NA |
Region | 1p13.3 |
Chromosome id | chr1 |
Chromosome position | 106887973 |
Reported gene | intergenic |
Mapped gene | LOC105378889 - PRMT6 |
Upstream gene id | 105378889 |
Downstream gene id | 55170 |
SNP gene ids | |
Upstream gene distance | 9671 |
Downstream gene distance | 168672 |
SNP risk allele | rs17440619-? |
SNPs | rs17440619 |
Merged | |
SNP id current | 17440619 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | |
Or beta | 2.79 |
%95 Ci | [1.83-4.25] |
Platform | Illumina [4196861] (imputed) |
CNV | N |
Mapped trait | Dysphagia |
Mapped trait URI | http://purl.obolibrary.org/obo/HP_0002015 |
Study accession | GCST002995 |