Human SNP ID | rs3733655 |
---|---|
Human chromosome | chr4 |
Human SNP position | 31144396 |
Pig chromosome | chr8 |
Pig SNP position | 24733032 |
PubMed ID | 26674333 |
---|---|
Journal | Neurology |
Link | www.ncbi.nlm.nih.gov/pubmed/26674333 |
Study | Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke. |
Disease/Trait | White matter hyperintensities in ischemic stroke |
Initial sample | 3,670 European ancestry cases |
Replication sample | NA |
Region | 4p15.1 |
Chromosome id | chr4 |
Chromosome position | 31144396 |
Reported gene | PCDH7 |
Mapped gene | PCDH7 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 5099 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs3733655-A |
SNPs | rs3733655 |
Merged | |
SNP id current | 3733655 |
Context | 3_prime_UTR_variant |
Intergenic | 0 |
Allele frequency | 0.64 |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | 1.13 |
%95 Ci | [1.07鈥?.18] |
Platform | Affymetrix, Illumina [7567914] (imputed) |
CNV | N |
Mapped trait | Ischemic stroke, white matter hyperintensity measurement |
Mapped trait URI | http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0005665 |
Study accession | GCST003245 |