Human SNP ID | rs41389746 |
---|---|
Human chromosome | chr16 |
Human SNP position | 82604613 |
Pig chromosome | chr6 |
Pig SNP position | 6378009 |
PubMed ID | 26718567 |
---|---|
Journal | Neurology |
Link | www.ncbi.nlm.nih.gov/pubmed/26718567 |
Study | Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke. |
Disease/Trait | Creatinine levels in ischemic stroke |
Initial sample | 1,725 European ancestry cases, 258 African ancestry cases, 117 cases |
Replication sample | NA |
Region | 16q23.3 |
Chromosome id | chr16 |
Chromosome position | 82604613 |
Reported gene | NR |
Mapped gene | LOC101928392 - CDH13 |
Upstream gene id | 101928392 |
Downstream gene id | 1012 |
SNP gene ids | |
Upstream gene distance | 29152 |
Downstream gene distance | 22181 |
SNP risk allele | rs41389746-? |
SNPs | rs41389746 |
Merged | |
SNP id current | 41389746 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [7500450] (imputed) |
CNV | N |
Mapped trait | Ischemic stroke, serum creatinine measurement |
Mapped trait URI | http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0004518 |
Study accession | GCST003213 |