rs1057519847
|
|
72
|
0.570 |
0.560 |
7 |
55191821 |
missense variant
|
CT/AG
|
mnv |
|
|
0.030 |
1.000 |
3 |
2007 |
2013 |
rs1057519848
|
|
72
|
0.570 |
0.560 |
7 |
55191822 |
missense variant
|
TG/GT
|
mnv |
|
|
0.030 |
1.000 |
3 |
2007 |
2013 |
rs121434568
|
|
73
|
0.568 |
0.560 |
7 |
55191822 |
missense variant
|
T/A;G
|
snv |
|
|
0.030 |
1.000 |
3 |
2007 |
2013 |
rs401681
|
|
42
|
0.620 |
0.640 |
5 |
1321972 |
intron variant
|
C/T
|
snv |
|
0.48
|
0.020 |
0.500 |
2 |
2013 |
2014 |
rs4324798
|
|
8
|
0.790 |
0.240 |
6 |
28808340 |
intergenic variant
|
G/A
|
snv |
|
7.2E-02
|
0.020 |
1.000 |
2 |
2010 |
2011 |
rs10118776
|
|
1
|
1.000 |
0.080 |
9 |
6227418 |
intron variant
|
G/A
|
snv |
|
0.94
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs1023835002
|
|
10
|
0.763 |
0.280 |
15 |
44711547 |
start lost
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1045494
|
|
3
|
0.882 |
0.120 |
2 |
201287058 |
3 prime UTR variant
|
T/C
|
snv |
|
0.10
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs1057519747
|
|
23
|
0.716 |
0.280 |
17 |
7675094 |
missense variant
|
A/C;G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1057519877
|
|
10
|
0.763 |
0.280 |
15 |
44711549 |
start lost
|
G/A
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1057519879
|
|
10
|
0.763 |
0.280 |
15 |
44711548 |
start lost
|
T/C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1057519927
|
|
19
|
0.716 |
0.240 |
3 |
179218295 |
missense variant
|
A/C;G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1057519985
|
|
16
|
0.724 |
0.360 |
17 |
7673763 |
missense variant
|
T/A;C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1057519989
|
|
17
|
0.732 |
0.240 |
17 |
7674233 |
missense variant
|
C/A;G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1057520003
|
|
20
|
0.695 |
0.320 |
17 |
7675996 |
missense variant
|
T/G
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1057520005
|
|
14
|
0.742 |
0.360 |
17 |
7673800 |
missense variant
|
C/A;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1057520006
|
|
14
|
0.752 |
0.240 |
17 |
7673799 |
missense variant
|
A/C;G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs10937405
|
|
9
|
0.807 |
0.080 |
3 |
189665394 |
intron variant
|
C/T
|
snv |
|
0.38
|
0.010 |
< 0.001 |
1 |
2011 |
2011 |
rs114033761
|
|
1
|
1.000 |
0.080 |
6 |
31093784 |
regulatory region variant
|
T/C
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs116427960
|
|
3
|
0.925 |
0.120 |
6 |
31351449 |
intron variant
|
C/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs117729306
|
|
1
|
1.000 |
0.080 |
11 |
8465623 |
non coding transcript exon variant
|
T/C
|
snv |
|
7.3E-03
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs121909229
|
|
23
|
0.683 |
0.400 |
10 |
87933148 |
missense variant
|
G/A;C;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs121912660
|
|
26
|
0.683 |
0.240 |
17 |
7673781 |
missense variant
|
C/A;G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs121913273
|
|
44
|
0.605 |
0.440 |
3 |
179218294 |
missense variant
|
G/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs121913274
|
|
33
|
0.645 |
0.320 |
3 |
179218304 |
missense variant
|
A/C;G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |