Human SNP ID | rs2827025 |
---|---|
Human chromosome | chr21 |
Human SNP position | 21772282 |
Pig chromosome | chr13 |
Pig SNP position | 195762709 |
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 | 21q21.1 |
Chromosome id | chr21 |
Chromosome position | 21772282 |
Reported gene | NR |
Mapped gene | LINC01425 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 101927821 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2827025-? |
SNPs | rs2827025 |
Merged | |
SNP id current | 2827025 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | |
Or beta | 2.521 |
%95 Ci | [NR] |
Platform | Illumina [4196861] (imputed) |
CNV | N |
Mapped trait | Dysphagia |
Mapped trait URI | http://purl.obolibrary.org/obo/HP_0002015 |
Study accession | GCST002995 |