NM_001370298.3(FGD4):c.1716G>A (p.Arg572=)
|
rs10844253
|
0.27488
|
NM_001370298.3(FGD4):c.1929G>A (p.Ala643=)
|
rs11052110
|
0.25239
|
NM_001370298.3(FGD4):c.2047-7T>C
|
rs11052113
|
0.15340
|
NM_001370298.3(FGD4):c.1404+8G>A
|
rs12823621
|
0.07737
|
NM_001370298.3(FGD4):c.167-29719A>G
|
rs17537634
|
0.01912
|
NM_001370298.3(FGD4):c.1926T>C (p.Ser642=)
|
rs60803891
|
0.01632
|
NM_001370298.3(FGD4):c.1954-8T>C
|
rs115061722
|
0.01466
|
NM_001370298.3(FGD4):c.1143G>A (p.Ser381=)
|
rs34555341
|
0.00555
|
NM_001370298.3(FGD4):c.1971C>T (p.Ile657=)
|
rs61748364
|
0.00526
|
NM_001370298.3(FGD4):c.1296C>T (p.Phe432=)
|
rs151083690
|
0.00230
|
NM_001370298.3(FGD4):c.1777C>A (p.Pro593Thr)
|
rs138160928
|
0.00168
|
NM_001370298.3(FGD4):c.666A>T (p.Ala222=)
|
rs139357821
|
0.00161
|
NM_001370298.3(FGD4):c.2560G>A (p.Val854Met)
|
rs61753359
|
0.00131
|
NM_001370298.3(FGD4):c.2070C>G (p.Ala690=)
|
rs188104446
|
0.00106
|
NM_001370298.3(FGD4):c.1075G>A (p.Val359Ile)
|
rs528790143
|
0.00050
|
NM_001370298.3(FGD4):c.1923-7A>G
|
rs200542541
|
0.00021
|
NM_001370298.3(FGD4):c.2193C>T (p.Ser731=)
|
rs147136365
|
0.00021
|
NM_001370298.3(FGD4):c.1404+10C>T
|
rs374656859
|
0.00016
|
NM_001370298.3(FGD4):c.1759A>G (p.Met587Val)
|
rs201186597
|
0.00016
|
NM_001370298.3(FGD4):c.1409A>G (p.Gln470Arg)
|
rs200149526
|
0.00005
|
NM_001370298.3(FGD4):c.1602+13C>T
|
rs557373932
|
0.00005
|
NM_001370298.3(FGD4):c.176C>G (p.Thr59Ser)
|
rs187853007
|
0.00004
|
NM_001370298.3(FGD4):c.2373G>A (p.Glu791=)
|
rs201822384
|
0.00003
|
NM_001370298.3(FGD4):c.2172+8A>T
|
rs761674021
|
0.00002
|
NM_001370298.3(FGD4):c.2148G>A (p.Arg716=)
|
rs372451301
|
0.00001
|
NM_001370298.3(FGD4):c.319+1G>A
|
rs1057518446
|
0.00001
|
NM_001370298.3(FGD4):c.1509G>T (p.Leu503Phe)
|
rs1555216969
|
|
NM_001370298.3(FGD4):c.166+1G>A
|
|
|
NM_001370298.3(FGD4):c.1839G>A (p.Met613Ile)
|
|
|
NM_001370298.3(FGD4):c.1971C>A (p.Ile657=)
|
rs61748364
|
|
NM_001370298.3(FGD4):c.2122C>A (p.Pro708Thr)
|
rs144693221
|
|
NM_001370298.3(FGD4):c.2451C>T (p.Pro817=)
|
rs1314359233
|
|
NM_001370298.3(FGD4):c.376C>A (p.Pro126Thr)
|
rs199744649
|
|
NM_001370298.3(FGD4):c.846C>G (p.Asp282Glu)
|
rs904582
|
|
NM_001370298.3(FGD4):c.846C>T (p.Asp282=)
|
rs904582
|
|