rs113624356
|
|
22
|
0.724 |
0.400 |
11 |
66526181 |
missense variant
|
T/G
|
snv |
1.5E-03
|
2.1E-03
|
0.700 |
|
0 |
|
|
rs113993959
|
|
25
|
0.677 |
0.280 |
7 |
117587778 |
stop gained
|
G/A;T
|
snv |
8.0E-06;
3.4E-04
|
|
0.700 |
|
0 |
|
|
rs1178187217
|
|
38
|
0.683 |
0.480 |
7 |
21600085 |
missense variant
|
G/A;T
|
snv |
4.3E-06
|
|
0.700 |
|
0 |
|
|
rs1294950721
|
|
27
|
0.807 |
0.360 |
20 |
10645355 |
splice donor variant
|
C/A;T
|
snv |
|
7.0E-06
|
0.700 |
|
0 |
|
|
rs137854539
|
|
28
|
0.716 |
0.520 |
20 |
58903703 |
missense variant
|
C/T
|
snv |
|
|
0.700 |
|
0 |
|
|
rs1441937959
|
|
20
|
0.763 |
0.280 |
15 |
82240555 |
missense variant
|
T/C
|
snv |
8.2E-06
|
|
0.700 |
|
0 |
|
|
rs1554317002
|
|
45
|
0.724 |
0.440 |
7 |
39950821 |
frameshift variant
|
C/-
|
delins |
|
|
0.700 |
|
0 |
|
|
rs1555549674
|
|
6
|
0.882 |
0.240 |
17 |
42223402 |
missense variant
|
T/G
|
snv |
|
|
0.700 |
|
0 |
|
|
rs201943194
|
|
38
|
0.683 |
0.480 |
7 |
21710596 |
stop gained
|
C/T
|
snv |
8.5E-05
|
8.4E-05
|
0.700 |
|
0 |
|
|
rs559979281
|
|
23
|
0.742 |
0.440 |
2 |
121530892 |
non coding transcript exon variant
|
C/G;T
|
snv |
7.7E-06;
2.3E-05;
3.5E-04
|
|
0.700 |
|
0 |
|
|
rs74597325
|
|
18
|
0.708 |
0.320 |
7 |
117587811 |
stop gained
|
C/G;T
|
snv |
6.8E-05
|
|
0.700 |
|
0 |
|
|
rs80359473
|
|
12
|
0.807 |
0.400 |
13 |
32339288 |
frameshift variant
|
GAAA/-
|
delins |
|
|
0.700 |
|
0 |
|
|
rs863225422
|
|
23
|
0.742 |
0.440 |
2 |
121530927 |
non coding transcript exon variant
|
G/A
|
snv |
4.6E-05;
7.7E-06
|
4.9E-05
|
0.700 |
|
0 |
|
|
rs866294686
|
|
43
|
0.683 |
0.480 |
10 |
102657073 |
stop gained
|
C/A;T
|
snv |
|
|
0.700 |
|
0 |
|
|
rs869312169
|
|
3
|
0.925 |
0.080 |
9 |
452067 |
frameshift variant
|
-/T
|
delins |
|
|
0.700 |
|
0 |
|
|
rs1300030496
|
|
1
|
1.000 |
0.080 |
2 |
8731757 |
missense variant
|
T/G
|
snv |
4.0E-06
|
|
0.010 |
< 0.001 |
1 |
1998 |
1998 |
rs1557055405
|
|
21
|
0.807 |
0.400 |
X |
153743532 |
missense variant
|
T/A
|
snv |
|
|
0.700 |
1.000 |
1 |
1998 |
1998 |
rs1267969615
|
|
100
|
0.532 |
0.760 |
17 |
63490960 |
missense variant
|
T/C
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
1999 |
1999 |
rs699
|
|
134
|
0.501 |
0.800 |
1 |
230710048 |
missense variant
|
A/G
|
snv |
0.55
|
0.58
|
0.010 |
1.000 |
1 |
1999 |
1999 |
rs1051931
|
|
19
|
0.708 |
0.400 |
6 |
46705206 |
missense variant
|
A/G
|
snv |
0.81
|
0.79
|
0.010 |
1.000 |
1 |
2000 |
2000 |
rs10800812
|
|
1
|
1.000 |
0.080 |
1 |
202086810 |
intergenic variant
|
A/G
|
snv |
|
0.77
|
0.700 |
1.000 |
1 |
2000 |
2000 |
rs1229598
|
|
1
|
1.000 |
0.080 |
18 |
56267556 |
regulatory region variant
|
A/C;G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2000 |
2000 |
rs1320896171
|
|
3
|
0.882 |
0.120 |
17 |
2680294 |
missense variant
|
C/T
|
snv |
|
7.0E-06
|
0.010 |
1.000 |
1 |
2000 |
2000 |
rs17064520
|
|
1
|
1.000 |
0.080 |
18 |
58242398 |
intron variant
|
C/T
|
snv |
|
0.19
|
0.700 |
1.000 |
1 |
2000 |
2000 |
rs1805018
|
|
6
|
0.827 |
0.200 |
6 |
46711566 |
missense variant
|
A/G
|
snv |
6.8E-02
|
0.10
|
0.010 |
1.000 |
1 |
2000 |
2000 |