Human SNP ID | rs41314453 |
---|---|
Human chromosome | chr9 |
Human SNP position | 133442704 |
Pig chromosome | chr1 |
Pig SNP position | 307015787 |
PubMed ID | 25934476 |
---|---|
Journal | Blood |
Link | www.ncbi.nlm.nih.gov/pubmed/25934476 |
Study | Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity. |
Disease/Trait | ADAMTS13 activity |
Initial sample | 3,423 European ancestry individuals |
Replication sample | 2,025 European ancestry individuals |
Region | 9q34.2 |
Chromosome id | chr9 |
Chromosome position | 133442704 |
Reported gene | ADAMTS13 |
Mapped gene | ADAMTS13 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 11093 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs41314453-T |
SNPs | rs41314453 |
Merged | 0 |
SNP id current | 41314453 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | 0.0188 |
P value | 1E-63 |
Pvalue mlog | 63 |
P value text | |
Or beta | 21.7 |
%95 Ci | unit decrease |
Platform | Illumina [8237900] (imputed) |
CNV | N |
Mapped trait | ADAMTS13 activity measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0006955 |
Study accession | GCST002881 |