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_000552.3(VWF):c.-1303G>A
|
rs7965413
|
0.53288
|
NM_000552.5(VWF):c.3240T>C (p.Tyr1080=)
|
rs4021576
|
0.09832
|
NM_000552.5(VWF):c.3379+7A>C
|
rs113446850
|
0.09700
|
NM_000552.5(VWF):c.4665A>C (p.Ala1555=)
|
rs1800384
|
0.08554
|
NM_000552.5(VWF):c.4693G>T (p.Val1565Leu)
|
rs1800385
|
0.08527
|
NM_000552.5(VWF):c.3579T>C (p.Pro1193=)
|
rs16933969
|
0.06947
|
NM_000552.5(VWF):c.6554G>A (p.Arg2185Gln)
|
rs2229446
|
0.06069
|
NM_000552.5(VWF):c.3426T>C (p.Cys1142=)
|
rs535693463
|
0.05771
|
NM_000552.5(VWF):c.2220G>A (p.Met740Ile)
|
rs2228317
|
0.05696
|
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.6345T>A (p.Thr2115=)
|
rs11537642
|
0.04599
|
NM_000552.5(VWF):c.3795G>A (p.Pro1265=)
|
rs2228319
|
0.03767
|
NM_000552.5(VWF):c.4138A>G (p.Ile1380Val)
|
rs11063988
|
0.03649
|
NM_000552.5(VWF):c.2451T>A (p.His817Gln)
|
rs57950734
|
0.03591
|
NM_000552.5(VWF):c.4304A>G (p.Asn1435Ser)
|
rs11063987
|
0.03448
|
NM_000552.5(VWF):c.7997C>T (p.Thr2666Met)
|
rs78353028
|
0.02215
|
NM_000552.5(VWF):c.1794C>T (p.Ala598=)
|
rs35302737
|
0.02100
|
NM_000552.5(VWF):c.1433-10T>C
|
rs66722092
|
0.01853
|
NM_000552.5(VWF):c.5667C>T (p.Pro1889=)
|
rs56981471
|
0.01850
|
NM_000552.5(VWF):c.56-40C>T
|
rs113081282
|
0.01669
|
NM_000552.5(VWF):c.390C>T (p.Ser130=)
|
rs2229444
|
0.01260
|
NM_000552.5(VWF):c.7698G>A (p.Lys2566=)
|
rs16932285
|
0.00947
|
NM_000552.5(VWF):c.5277C>T (p.Asp1759=)
|
rs41276736
|
0.00826
|
NM_000552.5(VWF):c.5173C>T (p.Pro1725Ser)
|
rs78302129
|
0.00774
|
NM_000552.5(VWF):c.2510C>A (p.Ala837Asp)
|
rs75645183
|
0.00739
|
NM_000552.5(VWF):c.5515T>C (p.Leu1839=)
|
rs141134620
|
0.00734
|
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.7771-10C>T
|
rs189370859
|
0.00565
|
NM_000552.5(VWF):c.6187C>T (p.Pro2063Ser)
|
rs61750615
|
0.00437
|
NM_000552.5(VWF):c.5170+10C>T
|
rs61750601
|
0.00400
|
NM_000552.5(VWF):c.7362C>T (p.Thr2454=)
|
rs146504585
|
0.00038
|
NM_000552.5(VWF):c.3485_3486inv (p.Pro1162Leu)
|
|
|
NM_000552.5(VWF):c.3692A>C (p.Asn1231Thr)
|
rs61749368
|
|
NM_000552.5(VWF):c.4414G>C (p.Asp1472His)
|
rs1800383
|
|
NM_000552.5(VWF):c.5171-9del
|
rs199893035
|
|