Human SNP ID | rs4980079 |
---|---|
Human chromosome | chr10 |
Human SNP position | 79434463 |
Pig chromosome | JH118438-1 |
Pig SNP position | 47944 |
PubMed ID | 26154020 |
---|---|
Journal | Neurobiol Aging |
Link | www.ncbi.nlm.nih.gov/pubmed/26154020 |
Study | A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia. |
Disease/Trait | Frontotemporal dementia |
Initial sample | 530 European ancestry cases, 926 European ancestry controls |
Replication sample | NA |
Region | 10q22.3 |
Chromosome id | chr10 |
Chromosome position | 79434463 |
Reported gene | ZCCHC24 |
Mapped gene | ZCCHC24 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 219654 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4980079-T |
SNPs | rs4980079 |
Merged | |
SNP id current | 4980079 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.45 |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | |
Or beta | 1.46 |
%95 Ci | [1.30-1.62] |
Platform | Illumina [2292247] (imputed) |
CNV | N |
Mapped trait | Frontotemporal dementia |
Mapped trait URI | http://www.orpha.net/ORDO/Orphanet_282 |
Study accession | GCST002960 |