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VWF

From SNPedia

is agene
is mentioned by
Full namevon Willebrand factor
EntrezGene7450
PheGenI7450
VariationViewer7450
ClinVarVWF
GeneCardsVWF
dbSNP7450
SADR7450
HugeNav7450
wikipediaVWF
googleVWF
gopubmedVWF
EVSVWF
HEFalMpVWF
MyGene2VWF
23andMeVWF
UniProtP04275
EnsemblENSG00000110799
OMIM613160
# SNPs89
 Max MagnitudeChromosome positionSummary
i30024556,127,833
i30027976,131,126
i50045186,131,999
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
rs106385606,044,368
rs10638576,044,348
rs116149126,039,389
rs12196489446,036,488
rs12196489536,021,960
rs18003786,063,036
rs180038006,029,429
rs180038206,019,222
rs180038636,018,667
rs2162936,044,493
rs2163116,019,277
rs21632106,034,818
rs222944605,993,906
rs22391536,077,501
rs236333736,023,630
rs26760732636,022,841
rs26760735346,016,197
rs2893487906,021,960
rs3397890136,031,493
rs3423028805,993,928
... 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.