NM_000552.5(VWF):c.7239T>C (p.Thr2413=)
|
rs216867
|
0.84456
|
NM_000552.5(VWF):c.6799-14C>T
|
rs177702
|
0.76003
|
NM_000552.5(VWF):c.4641T>C (p.Thr1547=)
|
rs216310
|
0.71518
|
NM_000552.5(VWF):c.4141A>G (p.Thr1381Ala)
|
rs216311
|
0.71493
|
NM_000552.5(VWF):c.1451A>G (p.His484Arg)
|
rs1800378
|
0.51348
|
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.5844C>T (p.Cys1948=)
|
rs216902
|
0.37406
|
NM_000552.5(VWF):c.7082-7C>T
|
rs216868
|
0.26357
|
NM_000552.5(VWF):c.1182A>C (p.Ser394=)
|
rs1800376
|
0.24101
|
NM_000552.5(VWF):c.1173A>T (p.Thr391=)
|
rs1800375
|
0.23172
|
NM_000552.5(VWF):c.6846A>G (p.Thr2282=)
|
rs1053523
|
0.15412
|
NM_000552.5(VWF):c.954T>A (p.Asn318Lys)
|
rs1800387
|
0.15296
|
NM_000552.5(VWF):c.3258C>T (p.Tyr1086=)
|
rs112634786
|
0.04897
|
NM_000552.5(VWF):c.3414C>T (p.Asn1138=)
|
rs560397436
|
0.04853
|
NM_000552.5(VWF):c.8113G>A (p.Gly2705Arg)
|
rs7962217
|
0.04240
|
NM_000552.5(VWF):c.6798+14C>T
|
rs7315124
|
0.03357
|
NM_000552.5(VWF):c.5843-8C>G
|
rs34444862
|
0.01303
|
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.7887+12T>C
|
rs55687637
|
0.00814
|
NM_000552.5(VWF):c.2561G>A (p.Arg854Gln)
|
rs41276738
|
0.00377
|
NM_000552.5(VWF):c.7940C>T (p.Thr2647Met)
|
rs61751302
|
0.00352
|
NM_000552.5(VWF):c.114C>T (p.Phe38=)
|
rs2229443
|
0.00241
|
NM_000552.5(VWF):c.4751A>G (p.Tyr1584Cys)
|
rs1800386
|
0.00237
|
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.4443G>T (p.Gly1481=)
|
rs144796763
|
0.00101
|
NM_000552.5(VWF):c.5278G>A (p.Val1760Ile)
|
rs61750604
|
0.00094
|
NM_000552.5(VWF):c.7344C>T (p.Cys2448=)
|
rs55944252
|
0.00046
|
NM_000552.5(VWF):c.6377T>C (p.Ile2126Thr)
|
rs71579338
|
0.00025
|
NM_000552.5(VWF):c.5533G>A (p.Asp1845Asn)
|
rs201548925
|
0.00012
|
NM_000552.5(VWF):c.7493C>A (p.Ala2498Asp)
|
rs369669154
|
0.00004
|
NM_000552.5(VWF):c.7603C>T (p.Arg2535Ter)
|
rs61751296
|
0.00001
|
NM_000552.5(VWF):c.4105T>A (p.Phe1369Ile)
|
rs61750069
|
|
NM_000552.5(VWF):c.4414G>C (p.Asp1472His)
|
rs1800383
|
|
NM_000552.5(VWF):c.4789C>T (p.Arg1597Trp)
|
rs61750117
|
|