VWF
From SNPedia
is a | gene |
is | mentioned by |
Full name | von Willebrand factor |
EntrezGene | 7450 |
PheGenI | 7450 |
VariationViewer | 7450 |
ClinVar | VWF |
GeneCards | VWF |
dbSNP | 7450 |
Diseases | VWF |
SADR | 7450 |
HugeNav | 7450 |
wikipedia | VWF |
VWF | |
gopubmed | VWF |
EVS | VWF |
HEFalMp | VWF |
MyGene2 | VWF |
23andMe | VWF |
UniProt | P04275 |
Ensembl | ENSG00000110799 |
OMIM | 613160 |
# SNPs | 102 |
Max Magnitude | Chromosome position | Summary | |
---|---|---|---|
i3002455 | 6,127,833 | ||
i3002797 | 6,131,126 | ||
i5004518 | 6,131,999 | ||
i5039448 | |||
i5039483 | |||
i5049057 | |||
i5049076 | |||
i5049104 | |||
i5049115 | |||
i5049117 | |||
i5049144 | |||
i5049145 | |||
i5049157 | |||
i5049159 | |||
i5049161 | |||
i5049165 | |||
i5049172 | |||
i5049192 | |||
i5049208 | |||
i5049228 | |||
i5049258 | |||
i5049266 | |||
i5049282 | |||
i5049284 | |||
i5049289 | |||
i5049314 | |||
i5049327 | |||
i5049338 | |||
i5049343 | |||
i5049344 | |||
rs1063856 | 0 | 6,044,368 | |
rs1063857 | 0 | 6,044,348 | |
rs11614912 | 0 | 6,039,389 | |
rs121964894 | 4 | 6,036,488 | |
rs121964895 | 3.5 | 6,021,960 | |
rs1800378 | 0 | 6,063,036 | |
rs1800380 | 0 | 6,029,429 | |
rs1800382 | 0 | 6,019,222 | |
rs1800386 | 3 | 6,018,667 | |
rs216293 | 0 | 6,044,493 | |
rs216311 | 0 | 6,019,277 | |
rs216321 | 0 | 6,034,818 | |
rs2229446 | 0 | 5,993,906 | |
rs2239144 | 0 | 6,087,017 | |
rs2239153 | 0 | 6,077,501 | |
rs2363337 | 3 | 6,023,630 | |
rs267607326 | 3.5 | 6,022,841 | |
rs267607353 | 4 | 6,016,197 | |
rs28934879 | 0 | 6,021,960 | |
rs33978901 | 3 | 6,031,493 | |
... further results |
The VWF gene encodes the von Willebrand factor. This glycoprotein functions as both an antihemophilic factor carrier and a platelet-vessel wall mediator in the blood coagulation system. It is crucial to the hemostasis process. Mutations in the VWF gene or deficiencies in the protein result in von Willebrand disease.