ClinVar Miner

List of variants in gene VWF reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP gnomAD frequency
NM_000552.5(VWF):c.7771-173T>C rs216851 0.99629
NM_000552.5(VWF):c.220+52T>C rs6489694 0.99048
NM_000552.5(VWF):c.2282-133T>C rs216294 0.91760
NM_000552.5(VWF):c.2547-177A>C rs669667 0.91602
NM_000552.5(VWF):c.2547-172A>G rs499648 0.91599
NM_000552.5(VWF):c.2546+329T>C rs216324 0.91562
NM_000552.5(VWF):c.4641T>C (p.Thr1547=) rs216310 0.71518
NM_000552.5(VWF):c.2546+25C>T rs216325 0.70354
NM_000552.5(VWF):c.7288-87T>C rs216855 0.68144
NM_000552.5(VWF):c.7548+188C>G rs2238110 0.67644
NM_000552.5(VWF):c.7548+170C>T rs11063965 0.67597
NM_000552.5(VWF):c.7548+231A>G rs10849365 0.66445
NM_000552.5(VWF):c.3675-75A>G rs216312 0.62640
NM_000552.5(VWF):c.56-319T>C rs1814250 0.62410
NM_000552.5(VWF):c.5665-118G>A rs216305 0.58621
NM_000552.5(VWF):c.6598+264C>T rs216898 0.57469
NM_000552.5(VWF):c.1433-173A>G rs2239158 0.56688
NM_000552.5(VWF):c.6598+198A>G rs76092459 0.55985
NM_000552.5(VWF):c.5843-111A>G rs216903 0.55941
NM_000552.5(VWF):c.533-153del rs5796209 0.52751
NM_000552.5(VWF):c.6798+189G>A rs216896 0.51412
NM_000552.5(VWF):c.6063+300C>T rs216901 0.51097
NM_000552.5(VWF):c.1-64C>T rs2286608 0.49101
NM_000552.5(VWF):c.1548T>C (p.Tyr516=) rs1800379 0.41956
NM_000552.5(VWF):c.2365A>G (p.Thr789Ala) rs1063856 0.40814
NM_000552.5(VWF):c.2385T>C (p.Tyr795=) rs1063857 0.40791
NM_000552.5(VWF):c.2282-121T>C rs1558519 0.40764
NM_000552.5(VWF):c.2282-122G>A rs1558520 0.40764
NM_000552.5(VWF):c.6598+200A>G rs78432670 0.30739
NM_000552.5(VWF):c.1946-226A>G rs73034900 0.26615
NM_000552.5(VWF):c.6976+129C>T rs24177 0.26574
NM_000552.5(VWF):c.2880G>A (p.Arg960=) rs1800380 0.25897
NM_000552.5(VWF):c.5053+130A>C rs17491418 0.24188
NM_000552.5(VWF):c.6598+213C>T rs216899 0.19827
NM_000552.5(VWF):c.7287+127A>G rs216866 0.16311
NM_000552.5(VWF):c.6977-142C>T rs2192205 0.16251
NM_000552.5(VWF):c.954T>A (p.Asn318Lys) rs1800387 0.15296
NM_000552.5(VWF):c.1411G>A (p.Val471Ile) rs1800377 0.11338
NM_000552.5(VWF):c.657+11A>C rs7980045 0.10566
NM_000552.5(VWF):c.7288-19C>T rs3819540 0.08253
NM_000552.5(VWF):c.2555= (p.Gln852=) rs216321 0.08026
NM_000552.5(VWF):c.7081+298C>A rs2236774 0.07841
NM_000552.5(VWF):c.6064-225G>A rs12099542 0.07519
NM_000552.5(VWF):c.6063+25G>A rs3741906 0.07461
NM_000552.5(VWF):c.6799-106G>C rs11063974 0.07163
NM_000552.5(VWF):c.7287+60C>T rs2286937 0.07132
NM_000552.5(VWF):c.7288-21C>T rs3819539 0.07127
NM_000552.5(VWF):c.7081+281G>A rs2236773 0.07125
NM_000552.5(VWF):c.6976+59C>T rs2070885 0.07075
NM_000552.5(VWF):c.6976+259A>G rs2070887 0.07070
NM_000552.5(VWF):c.6598+121C>T rs10849376 0.07056
NM_000552.5(VWF):c.6902-210G>C rs2070883 0.07049
NM_000552.5(VWF):c.6902-105G>A rs2070884 0.07043
NM_000552.5(VWF):c.6598+126G>A rs216900 0.06581
NM_000552.5(VWF):c.3426T>C (p.Cys1142=) rs535693463 0.05771
NM_000552.5(VWF):c.3486A>G (p.Pro1162=) rs546732699 0.05708
NM_000552.5(VWF):c.3414C>T (p.Asn1138=) rs560397436 0.04853
NM_000552.5(VWF):c.7682T>A (p.Phe2561Tyr) rs35335161 0.04046
NM_000552.5(VWF):c.390C>T (p.Ser130=) rs2229444 0.01260
NM_000552.5(VWF):c.2900G>A (p.Gly967Asp) rs141087261 0.00842
NM_000552.5(VWF):c.1433-128G>T rs2239159
NM_000552.5(VWF):c.1945+209G>C rs73036509
NM_000552.5(VWF):c.1946-17_1946-15dup rs10622288
NM_000552.5(VWF):c.2282-42C>A rs216293
NM_000552.5(VWF):c.2443-291C>T rs216326
NM_000552.5(VWF):c.2967+243dup rs71445694
NM_000552.5(VWF):c.5053+303_5053+304del rs67479635
NM_000552.5(VWF):c.5053+304del rs67479635
NM_000552.5(VWF):c.6976+146G>A rs2070886
NM_000552.5(VWF):c.6977-225TATC[3] rs10535241
NM_000552.5(VWF):c.7437+86dup rs5796198
NM_000552.5(VWF):c.7549-59A>C rs2270239

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