Human SNP ID | rs823128 |
---|---|
Human chromosome | chr1 |
Human SNP position | 205744250 |
Pig chromosome | chr9 |
Pig SNP position | 72695711 |
PubMed ID | 19915575 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/19915575 |
Study | Genome-wide association study reveals genetic risk underlying Parkinson__s disease. |
Disease/Trait | Parkinson__s disease |
Initial sample | 1,713 European ancestry cases, 3,978 European ancestry controls |
Replication sample | 3,361 European ancestry cases, 4,573 European ancestry controls |
Region | 1q32.1 |
Chromosome id | chr1 |
Chromosome position | 205744250 |
Reported gene | PARK16, NUCKS1 |
Mapped gene | NUCKS1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 64710 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs823128-A |
SNPs | rs823128 |
Merged | 0 |
SNP id current | 823128 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.97 |
P value | 0.00000007 |
Pvalue mlog | 7.15490195998574 |
P value text | |
Or beta | 1.52 |
%95 Ci | [NR] |
Platform | Illumina [463185] |
CNV | N |
Mapped trait | Parkinson__s disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0002508 |
Study accession | GCST000528 |