ClinVar Miner

List of variants in gene VWF reported as uncertain significance for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 112
Download table as spreadsheet
HGVS dbSNP
NM_000552.4(VWF):c.-107C>G rs886049747
NM_000552.4(VWF):c.-131G>C rs886049748
NM_000552.4(VWF):c.-72C>T rs886049746
NM_000552.4(VWF):c.1001G>A (p.Gly334Glu)
NM_000552.4(VWF):c.1051G>A (p.Val351Met) rs535978867
NM_000552.4(VWF):c.1077C>T (p.Pro359=) rs71582884
NM_000552.4(VWF):c.1142A>G (p.Asn381Ser) rs886049745
NM_000552.4(VWF):c.114C>T (p.Phe38=) rs2229443
NM_000552.4(VWF):c.1463C>G (p.Ala488Gly)
NM_000552.4(VWF):c.1514G>A (p.Arg505His)
NM_000552.4(VWF):c.1596C>T (p.Gly532=) rs111240043
NM_000552.4(VWF):c.1625C>G (p.Ala542Gly) rs141649383
NM_000552.4(VWF):c.1730-18_1730-12del rs756282321
NM_000552.4(VWF):c.1730-5C>T rs569984866
NM_000552.4(VWF):c.1752C>T (p.Cys584=) rs748584672
NM_000552.4(VWF):c.182T>C (p.Leu61Pro)
NM_000552.4(VWF):c.1841C>T (p.Ser614Phe)
NM_000552.4(VWF):c.1862G>C (p.Cys621Ser) rs886049744
NM_000552.4(VWF):c.1922C>T (p.Ala641Val) rs61754019
NM_000552.4(VWF):c.2025G>A (p.Pro675=) rs779045480
NM_000552.4(VWF):c.2103C>T (p.Cys701=) rs78995469
NM_000552.4(VWF):c.2281+13C>T rs183077797
NM_000552.4(VWF):c.2289G>A (p.Arg763=) rs886049743
NM_000552.4(VWF):c.2299T>C (p.Cys767Arg)
NM_000552.4(VWF):c.250C>T (p.Leu84Phe) rs372664002
NM_000552.4(VWF):c.2547-5C>T rs373203368
NM_000552.4(VWF):c.2570A>G (p.Asn857Ser) rs765163545
NM_000552.4(VWF):c.2686-7T>G
NM_000552.4(VWF):c.2981G>A (p.Gly994Asp)
NM_000552.4(VWF):c.3108+5G>A rs61748495
NM_000552.4(VWF):c.3162G>C (p.Thr1054=) rs754421736
NM_000552.4(VWF):c.3251G>A (p.Cys1084Tyr)
NM_000552.4(VWF):c.3379+12C>T rs374393996
NM_000552.4(VWF):c.3538+6G>T rs886049742
NM_000552.4(VWF):c.3539-15A>G rs748934603
NM_000552.4(VWF):c.3719C>T (p.Pro1240Leu) rs150576611
NM_000552.4(VWF):c.3720G>A (p.Pro1240=) rs141792415
NM_000552.4(VWF):c.3835G>A (p.Val1279Ile) rs61749376
NM_000552.4(VWF):c.3842T>C (p.Leu1281Pro)
NM_000552.4(VWF):c.391G>A (p.Gly131Ser) rs76505074
NM_000552.4(VWF):c.3952G>A (p.Val1318Met) rs372028373
NM_000552.4(VWF):c.4007G>A (p.Arg1336Gln) rs886049741
NM_000552.4(VWF):c.4027A>G (p.Ile1343Val) rs150923481
NM_000552.4(VWF):c.4103T>C (p.Ile1368Thr) rs199675425
NM_000552.4(VWF):c.4146G>T (p.Leu1382=)
NM_000552.4(VWF):c.435C>G (p.Asn145Lys)
NM_000552.4(VWF):c.4360G>A (p.Val1454Ile)
NM_000552.4(VWF):c.4457C>T (p.Ser1486Leu)
NM_000552.4(VWF):c.4622A>G (p.Gln1541Arg)
NM_000552.4(VWF):c.4727C>A (p.Thr1576Asn)
NM_000552.4(VWF):c.4834G>C (p.Ala1612Pro)
NM_000552.4(VWF):c.5049A>C (p.Ala1683=) rs79275181
NM_000552.4(VWF):c.5170+5G>A
NM_000552.4(VWF):c.5191T>A (p.Ser1731Thr) rs61750603
NM_000552.4(VWF):c.5277C>T (p.Asp1759=) rs41276736
NM_000552.4(VWF):c.5369C>T (p.Pro1790Leu) rs551649729
NM_000552.4(VWF):c.5493C>T (p.Tyr1831=) rs769268109
NM_000552.4(VWF):c.55+8C>A rs114713980
NM_000552.4(VWF):c.5533G>A (p.Asp1845Asn) rs201548925
NM_000552.4(VWF):c.5620+10A>G rs886049740
NM_000552.4(VWF):c.5664+15G>A rs7961539
NM_000552.4(VWF):c.5668G>A (p.Gly1890Arg)
NM_000552.4(VWF):c.5785A>T (p.Asn1929Tyr) rs149799233
NM_000552.4(VWF):c.5849G>A (p.Cys1950Tyr)
NM_000552.4(VWF):c.5851A>G (p.Thr1951Ala) rs144072210
NM_000552.4(VWF):c.5876T>G (p.Val1959Gly) rs886049739
NM_000552.4(VWF):c.6043G>A (p.Glu2015Lys) rs775806908
NM_000552.4(VWF):c.6196A>G (p.Asn2066Asp) rs886049738
NM_000552.4(VWF):c.6314C>T (p.Thr2105Ile)
NM_000552.4(VWF):c.6421G>A (p.Val2141Ile)
NM_000552.4(VWF):c.6433C>T (p.Pro2145Ser) rs61750618
NM_000552.4(VWF):c.6538T>C (p.Tyr2180His)
NM_000552.4(VWF):c.6572T>C (p.Val2191Ala) rs753731128
NM_000552.4(VWF):c.6611C>T (p.Pro2204Leu) rs777556669
NM_000552.4(VWF):c.6756G>A (p.Glu2252=) rs71581020
NM_000552.4(VWF):c.6762C>G (p.Cys2254Trp)
NM_000552.4(VWF):c.6798+13G>A rs201509264
NM_000552.4(VWF):c.6798+5G>A
NM_000552.4(VWF):c.6798+6A>G
NM_000552.4(VWF):c.6859C>T (p.Arg2287Trp) rs61750625
NM_000552.4(VWF):c.6902-5T>A rs112046757
NM_000552.4(VWF):c.6908C>T (p.Thr2303Met) rs149432685
NM_000552.4(VWF):c.6931C>T (p.Arg2311Cys) rs150725355
NM_000552.4(VWF):c.6976+11C>T rs751395078
NM_000552.4(VWF):c.7007C>T (p.Pro2336Leu) rs144769404
NM_000552.4(VWF):c.7082-13G>C rs71581025
NM_000552.4(VWF):c.7135C>T (p.Arg2379Cys) rs61751283
NM_000552.4(VWF):c.7240G>A (p.Ala2414Thr) rs754853953
NM_000552.4(VWF):c.7362C>T (p.Thr2454=) rs146504585
NM_000552.4(VWF):c.7429T>C (p.Cys2477Arg)
NM_000552.4(VWF):c.7483del (p.Leu2495fs) rs1229452874
NM_000552.4(VWF):c.7698G>A (p.Lys2566=) rs16932285
NM_000552.4(VWF):c.7729+8A>G rs775123891
NM_000552.4(VWF):c.7730-4C>G rs71581030
NM_000552.4(VWF):c.7790T>A (p.Ile2597Asn) rs886049737
NM_000552.4(VWF):c.7800C>T (p.Cys2600=) rs200209213
NM_000552.4(VWF):c.7887+12T>C rs55687637
NM_000552.4(VWF):c.792del (p.Cys265fs) rs1565853894
NM_000552.4(VWF):c.7940C>T (p.Thr2647Met) rs61751302
NM_000552.4(VWF):c.7947C>T (p.Cys2649=) rs748907832
NM_000552.4(VWF):c.7988G>C (p.Arg2663Pro) rs149834874
NM_000552.4(VWF):c.8052C>A (p.Tyr2684Ter) rs1565806829
NM_000552.4(VWF):c.8096A>G (p.His2699Arg) rs886049736
NM_000552.4(VWF):c.814G>C (p.Ala272Pro)
NM_000552.4(VWF):c.8155+8C>T rs886049735
NM_000552.4(VWF):c.8160G>A (p.Glu2720=) rs368802960
NM_000552.4(VWF):c.8215T>C (p.Cys2739Arg)
NM_000552.4(VWF):c.8275A>G (p.Met2759Val)
NM_000552.4(VWF):c.8276T>C (p.Met2759Thr)
NM_000552.4(VWF):c.8307C>A (p.Asp2769Glu)
NM_000552.4(VWF):c.8366C>G (p.Thr2789Ser) rs371036946
NM_000552.4(VWF):c.858C>T (p.Thr286=) rs776206258

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.