ClinVar Miner

List of variants in gene VWF reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000552.5(VWF):c.2365A>G (p.Thr789Ala) rs1063856 0.40814
NM_000552.5(VWF):c.7682T>A (p.Phe2561Tyr) rs35335161 0.04046
NM_000552.5(VWF):c.1596C>T (p.Gly532=) rs111240043 0.00251
NM_000552.5(VWF):c.114C>T (p.Phe38=) rs2229443 0.00241
NM_000552.5(VWF):c.385C>A (p.Leu129Met) rs61753991 0.00225
NM_000552.5(VWF):c.3789G>A (p.Ser1263=) rs199831474 0.00146
NM_000552.5(VWF):c.8079C>T (p.Cys2693=) rs41276732 0.00130
NM_000552.5(VWF):c.546G>A (p.Ser182=) rs143054357 0.00125
NM_000552.5(VWF):c.6756G>A (p.Glu2252=) rs71581020 0.00110
NM_000552.5(VWF):c.2586G>T (p.Val862=) rs34510401 0.00109
NM_000552.5(VWF):c.7082-13G>C rs71581025 0.00108
NM_000552.5(VWF):c.2739A>C (p.Gly913=) rs35191786 0.00102
NM_000552.5(VWF):c.5191T>A (p.Ser1731Thr) rs61750603 0.00101
NM_000552.5(VWF):c.1077C>T (p.Pro359=) rs71582884 0.00053
NM_000552.5(VWF):c.4173A>G (p.Gln1391=) rs145009516 0.00039
NM_000552.5(VWF):c.1519A>G (p.Arg507Gly) rs189409574 0.00019
NM_000552.5(VWF):c.8325T>C (p.Ser2775=) rs138588762 0.00019
NM_000552.5(VWF):c.858C>T (p.Thr286=) rs776206258 0.00011
NM_000552.5(VWF):c.8175C>T (p.Asn2725=) rs759147832 0.00004
NM_000552.5(VWF):c.1467C>T (p.Ser489=) rs377066810 0.00002
NM_000552.5(VWF):c.3144C>T (p.Asn1048=) rs201874365 0.00002
NM_000552.5(VWF):c.4800G>A (p.Ala1600=) rs201264909 0.00002
NM_000552.5(VWF):c.1059C>T (p.Ser353=)
NM_000552.5(VWF):c.2389C>T (p.Leu797=)
NM_000552.5(VWF):c.2694C>T (p.Cys898=)
NM_000552.5(VWF):c.3837C>T (p.Val1279=) rs748289333
NM_000552.5(VWF):c.4206G>A (p.Gln1402=)
NM_000552.5(VWF):c.4431T>C (p.Thr1477=)
NM_000552.5(VWF):c.4500G>A (p.Ala1500=)
NM_000552.5(VWF):c.4824C>T (p.Thr1608=) rs142635883
NM_000552.5(VWF):c.5700C>T (p.His1900=)
NM_000552.5(VWF):c.6825C>T (p.His2275=)
NM_000552.5(VWF):c.7988G>C (p.Arg2663Pro) rs149834874
NM_000552.5(VWF):c.8094A>G (p.Glu2698=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.