Human SNP ID | rs10922449 |
---|---|
Human chromosome | chr1 |
Human SNP position | 198554967 |
Pig chromosome | chr10 |
Pig SNP position | 26088796 |
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 | Thrombin-antithrombin complex levels in ischemic stroke |
Initial sample | up to 1,725 European ancestry cases, up to 258 African ancestry cases, up to 117 cases |
Replication sample | NA |
Region | 1q31.3 |
Chromosome id | chr1 |
Chromosome position | 198554967 |
Reported gene | NR |
Mapped gene | ATP6V1G3 - PTPRC |
Upstream gene id | 127124 |
Downstream gene id | 5788 |
SNP gene ids | |
Upstream gene distance | 14022 |
Downstream gene distance | 84001 |
SNP risk allele | rs10922449-? |
SNPs | rs10922449 |
Merged | |
SNP id current | 10922449 |
Context | regulatory_region_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 |
Mapped trait URI | http://purl.obolibrary.org/obo/HP_0002140 |
Study accession | GCST003233 |