ClinVar Miner

List of variants in gene VWF reported as likely benign for not provided

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Total variants: 95
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HGVS dbSNP gnomAD frequency
NM_000552.5(VWF):c.4641T>C (p.Thr1547=) rs216310 0.71518
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.7997C>T (p.Thr2666Met) rs78353028 0.02215
NM_000552.5(VWF):c.6902-5T>A rs112046757 0.01517
NM_000552.5(VWF):c.6532G>T (p.Ala2178Ser) rs34230288 0.01330
NM_000552.5(VWF):c.5843-8C>G rs34444862 0.01303
NM_000552.5(VWF):c.2771G>A (p.Arg924Gln) rs33978901 0.01237
NM_000552.5(VWF):c.5313G>T (p.Gly1771=) rs2229448 0.00914
NM_000552.5(VWF):c.2900G>A (p.Gly967Asp) rs141087261 0.00842
NM_000552.5(VWF):c.3686T>G (p.Val1229Gly) rs61749367 0.00656
NM_000552.5(VWF):c.391G>A (p.Gly131Ser) rs76505074 0.00651
NM_000552.5(VWF):c.55+8C>A rs114713980 0.00452
NM_000552.5(VWF):c.1037C>T (p.Thr346Ile) rs111971143 0.00436
NM_000552.5(VWF):c.7940C>T (p.Thr2647Met) rs61751302 0.00352
NM_000552.5(VWF):c.4457C>T (p.Ser1486Leu) rs149424724 0.00282
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.3089A>G (p.Gln1030Arg) rs145125264 0.00222
NM_000552.5(VWF):c.2103C>T (p.Cys701=) rs78995469 0.00185
NM_000552.5(VWF):c.1728G>T (p.Met576Ile) rs150146744 0.00155
NM_000552.5(VWF):c.3789G>A (p.Ser1263=) rs199831474 0.00146
NM_000552.5(VWF):c.6099C>T (p.Tyr2033=) rs55784921 0.00132
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.4443G>T (p.Gly1481=) rs144796763 0.00101
NM_000552.5(VWF):c.5191T>A (p.Ser1731Thr) rs61750603 0.00101
NM_000552.5(VWF):c.5312-19A>C rs200237834 0.00098
NM_000552.5(VWF):c.5278G>A (p.Val1760Ile) rs61750604 0.00094
NM_000552.5(VWF):c.3719C>T (p.Pro1240Leu) rs150576611 0.00060
NM_000552.5(VWF):c.4050G>A (p.Ala1350=) rs143459496 0.00056
NM_000552.5(VWF):c.1077C>T (p.Pro359=) rs71582884 0.00053
NM_000552.5(VWF):c.1614C>T (p.Pro538=) rs138268387 0.00046
NM_000552.5(VWF):c.7344C>T (p.Cys2448=) rs55944252 0.00046
NM_000552.5(VWF):c.1107C>G (p.Thr369=) rs149640698 0.00042
NM_000552.5(VWF):c.4173A>G (p.Gln1391=) rs145009516 0.00039
NM_000552.5(VWF):c.1410C>T (p.Asp470=) rs111867665 0.00038
NM_000552.5(VWF):c.6377T>C (p.Ile2126Thr) rs71579338 0.00025
NM_000552.5(VWF):c.1519A>G (p.Arg507Gly) rs189409574 0.00019
NM_000552.5(VWF):c.21C>T (p.Ala7=) rs144128523 0.00019
NM_000552.5(VWF):c.3291C>T (p.Cys1097=) rs149895348 0.00019
NM_000552.5(VWF):c.8325T>C (p.Ser2775=) rs138588762 0.00019
NM_000552.5(VWF):c.2943C>T (p.Ser981=) rs369031938 0.00012
NM_000552.5(VWF):c.5533G>A (p.Asp1845Asn) rs201548925 0.00012
NM_000552.5(VWF):c.858C>T (p.Thr286=) rs776206258 0.00011
NM_000552.5(VWF):c.1533+15G>A rs184217564 0.00010
NM_000552.5(VWF):c.6069G>A (p.Thr2023=) rs375810839 0.00009
NM_000552.5(VWF):c.3978C>T (p.His1326=) rs568918496 0.00008
NM_000552.5(VWF):c.8273C>T (p.Ala2758Val) rs144542595 0.00008
NM_000552.5(VWF):c.3675-14G>A rs1369248196 0.00006
NM_000552.5(VWF):c.609A>G (p.Ala203=) rs757836378 0.00006
NM_000552.5(VWF):c.1515C>T (p.Arg505=) rs377198574 0.00005
NM_000552.5(VWF):c.55+15G>A rs201377447 0.00005
NM_000552.5(VWF):c.6015C>T (p.Ile2005=) rs575042694 0.00004
NM_000552.5(VWF):c.8175C>T (p.Asn2725=) rs759147832 0.00004
NM_000552.5(VWF):c.1668C>T (p.His556=) rs531761442 0.00003
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.1083C>T (p.Thr361=)
NM_000552.5(VWF):c.1110-6dup rs534403271
NM_000552.5(VWF):c.1755G>A (p.Ala585=)
NM_000552.5(VWF):c.2295A>G (p.Leu765=)
NM_000552.5(VWF):c.2389C>T (p.Leu797=)
NM_000552.5(VWF):c.2610C>T (p.Ile870=)
NM_000552.5(VWF):c.2694C>T (p.Cys898=)
NM_000552.5(VWF):c.3303C>T (p.Cys1101=)
NM_000552.5(VWF):c.3692A>C (p.Asn1231Thr) rs61749368
NM_000552.5(VWF):c.3692A>G (p.Asn1231Ser) rs61749368
NM_000552.5(VWF):c.3735G>A (p.Val1245=)
NM_000552.5(VWF):c.3837C>T (p.Val1279=) rs748289333
NM_000552.5(VWF):c.4131C>T (p.Ala1377=)
NM_000552.5(VWF):c.4206G>A (p.Gln1402=)
NM_000552.5(VWF):c.4431T>C (p.Thr1477=)
NM_000552.5(VWF):c.4458G>A (p.Ser1486=)
NM_000552.5(VWF):c.4500G>A (p.Ala1500=)
NM_000552.5(VWF):c.4824C>T (p.Thr1608=) rs142635883
NM_000552.5(VWF):c.5004G>A (p.Arg1668=) rs61750597
NM_000552.5(VWF):c.5700C>T (p.His1900=)
NM_000552.5(VWF):c.6825C>T (p.His2275=)
NM_000552.5(VWF):c.6901+14C>T
NM_000552.5(VWF):c.7083C>G (p.Ala2361=)
NM_000552.5(VWF):c.7392C>T (p.Arg2464=)
NM_000552.5(VWF):c.7707G>A (p.Ala2569=)
NM_000552.5(VWF):c.7730-177G>T rs573460498
NM_000552.5(VWF):c.7987-13T>C
NM_000552.5(VWF):c.7988G>C (p.Arg2663Pro) rs149834874
NM_000552.5(VWF):c.8094A>G (p.Glu2698=)
NM_000552.5(VWF):c.8295C>T (p.Asn2765=)

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