NM_000552.5(VWF):c.4075G>A (p.Glu1359Lys)
|
rs61749407
|
0.00001
|
NM_000552.5(VWF):c.5765G>A (p.Gly1922Glu)
|
rs1048674696
|
0.00001
|
NM_000552.5(VWF):c.1110-1G>T
|
rs61754005
|
|
NM_000552.5(VWF):c.1730-1G>T
|
rs1591889534
|
|
NM_000552.5(VWF):c.1843dup (p.Cys615fs)
|
rs2136454246
|
|
NM_000552.5(VWF):c.1916G>A (p.Arg639His)
|
rs2136454101
|
|
NM_000552.5(VWF):c.2174A>G (p.His725Arg)
|
rs2136449433
|
|
NM_000552.5(VWF):c.2182A>G (p.Met728Val)
|
rs1944527524
|
|
NM_000552.5(VWF):c.2981G>T (p.Gly994Val)
|
rs1591867991
|
|
NM_000552.5(VWF):c.3157dup (p.Gln1053fs)
|
rs2136420496
|
|
NM_000552.5(VWF):c.3286G>C (p.Asp1096His)
|
rs748673885
|
|
NM_000552.5(VWF):c.3358_3359insC (p.Trp1120fs)
|
rs2136418339
|
|
NM_000552.5(VWF):c.3688G>A (p.Val1230Ile)
|
rs2136414039
|
|
NM_000552.5(VWF):c.3805_3806insT (p.Asp1269fs)
|
rs2136413792
|
|
NM_000552.5(VWF):c.3806A>T (p.Asp1269Val)
|
rs2136413788
|
|
NM_000552.5(VWF):c.3807T>A (p.Asp1269Glu)
|
rs2136413783
|
|
NM_000552.5(VWF):c.4163A>G (p.Gln1388Arg)
|
rs1944101095
|
|
NM_000552.5(VWF):c.4413del (p.Asp1472fs)
|
rs1565831817
|
|
NM_000552.5(VWF):c.4414G>A (p.Asp1472Asn)
|
rs1800383
|
|
NM_000552.5(VWF):c.4414del (p.Asp1472fs)
|
rs2136412581
|
|
NM_000552.5(VWF):c.4922G>A (p.Arg1641Lys)
|
rs1944088119
|
|
NM_000552.5(VWF):c.5029A>G (p.Ile1677Val)
|
rs1242618824
|
|
NM_000552.5(VWF):c.5694G>C (p.Gln1898His)
|
rs1218412177
|
|
NM_000552.5(VWF):c.5729C>T (p.Thr1910Ile)
|
rs2136403566
|
|
NM_000552.5(VWF):c.575C>T (p.Ala192Val)
|
rs2136500405
|
|
NM_000552.5(VWF):c.6123C>A (p.Asn2041Lys)
|
rs1943786371
|
|
NM_000552.5(VWF):c.6136A>G (p.Ile2046Val)
|
rs2136386032
|
|
NM_000552.5(VWF):c.6446A>G (p.Glu2149Gly)
|
rs1397931528
|
|
NM_000552.5(VWF):c.6449G>C (p.Cys2150Ser)
|
rs2136385448
|
|
NM_000552.5(VWF):c.6455A>G (p.Lys2152Arg)
|
rs2136385431
|
|
NM_000552.5(VWF):c.6677C>T (p.Ser2226Phe)
|
rs181987927
|
|
NM_000552.5(VWF):c.7114C>T (p.Pro2372Ser)
|
rs2136371404
|
|
NM_000552.5(VWF):c.7201T>G (p.Ser2401Ala)
|
rs2136371219
|
|
NM_000552.5(VWF):c.7712G>A (p.Cys2571Tyr)
|
rs1258347142
|
|
NM_000552.5(VWF):c.8195A>G (p.Gln2732Arg)
|
rs1443181806
|
|
NM_000552.5(VWF):c.8401G>A (p.Ala2801Thr)
|
rs2136336158
|
|
NM_000552.5(VWF):c.949del (p.Ile317fs)
|
rs2136472072
|
|
NM_000552.5(VWF):c.960G>A (p.Met320Ile)
|
rs2136472049
|
|