Human SNP ID | rs216303 |
---|---|
Human chromosome | chr12 |
Human SNP position | 6049879 |
Pig chromosome | chr5 |
Pig SNP position | 67048421 |
PubMed ID | 26486471 |
---|---|
Journal | Eur J Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/26486471 |
Study | Genome-wide association studies identify genetic loci for low von Willebrand factor levels. |
Disease/Trait | Low vWF levels |
Initial sample | up to 1,635 European ancestry individuals with low vWF levels, up to 33,286 European ancestry individuals with normal vWF levels |
Replication sample | NA |
Region | 12p13.31 |
Chromosome id | chr12 |
Chromosome position | 6049879 |
Reported gene | VWF |
Mapped gene | VWF |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 7450 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs216303-? |
SNPs | rs216303 |
Merged | |
SNP id current | 216303 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 5E-22 |
Pvalue mlog | 21.3010299956639 |
P value text | |
Or beta | 1.754386 |
%95 Ci | [1.56-1.96] |
Platform | Affymetrix, Illumina [~ 2600000] (imputed) |
CNV | N |
Mapped trait | von Willebrand factor measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004629 |
Study accession | GCST003210 |