Human SNP ID | rs415430 |
---|---|
Human chromosome | chr17 |
Human SNP position | 46781778 |
Pig chromosome | JH118614-1 |
Pig SNP position | 84580 |
PubMed ID | 21812969 |
---|---|
Journal | BMC Med Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/21812969 |
Study | Genome-wide association study identifies candidate genes for Parkinson__s disease in an Ashkenazi Jewish population. |
Disease/Trait | Parkinson__s disease |
Initial sample | 268 Ashkenazi Jewish cases, 178 Ashkenazi Jewish controls |
Replication sample | 1,782 European ancestry cases, 1,658 European ancestry controls |
Region | 17q21.31 |
Chromosome id | chr17 |
Chromosome position | 46781778 |
Reported gene | WNT3 |
Mapped gene | WNT3 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 7473 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs415430-T |
SNPs | rs415430 |
Merged | 0 |
SNP id current | 415430 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.786 |
P value | 0.0000007 |
Pvalue mlog | 6.15490195998574 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [525124] |
CNV | N |
Mapped trait | Parkinson__s disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0002508 |
Study accession | GCST001189 |