Human SNP ID | rs6783485 |
---|---|
Human chromosome | chr3 |
Human SNP position | 59442071 |
Pig chromosome | chr13 |
Pig SNP position | 45339204 |
PubMed ID | 26227905 |
---|---|
Journal | Mol Neurobiol |
Link | www.ncbi.nlm.nih.gov/pubmed/26227905 |
Study | A Pooling Genome-Wide Association Study Combining a Pathway Analysis for Typical Sporadic Parkinson__s Disease in the Han Population of Chinese Mainland. |
Disease/Trait | Parkinson__s disease |
Initial sample | 250 Han Chinese ancestry cases, 250 Han Chinese ancestry controls |
Replication sample | NA |
Region | 3p14.2 |
Chromosome id | chr3 |
Chromosome position | 59442071 |
Reported gene | C3orf67, LOC339902 |
Mapped gene | LOC105377110 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105377110 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs6783485-? |
SNPs | rs6783485 |
Merged | |
SNP id current | 6783485 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | 5 |
%95 Ci | [2.86-8.33] |
Platform | Illumina [862198] |
CNV | N |
Mapped trait | Parkinson__s disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0002508 |
Study accession | GCST003059 |