Human SNP ID | rs17497526 |
---|---|
Human chromosome | chr10 |
Human SNP position | 69820364 |
Pig chromosome | chr14 |
Pig SNP position | 78724886 |
PubMed ID | 23793441 |
---|---|
Journal | Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23793441 |
Study | Parkinson disease loci in the mid-western Amish. |
Disease/Trait | Parkinson__s disease |
Initial sample | 31 Amish cases, 767 Amish controls |
Replication sample | NA |
Region | 10q22.1 |
Chromosome id | chr10 |
Chromosome position | 69820364 |
Reported gene | COL13A1 |
Mapped gene | COL13A1, LOC105378347 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 1305, 105378347 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs17497526-G |
SNPs | rs17497526 |
Merged | 0 |
SNP id current | 17497526 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.15 |
P value | 0.0000006 |
Pvalue mlog | 6.22184874961635 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Affymetrix [622812] |
CNV | N |
Mapped trait | Parkinson__s disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0002508 |
Study accession | GCST002077 |