rs10118570
|
|
2
|
0.925 |
0.120 |
9 |
125714185 |
intergenic variant
|
G/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1042522
|
|
242
|
0.426 |
0.800 |
17 |
7676154 |
missense variant
|
G/C;T
|
snv |
0.67
|
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs1048943
|
|
88
|
0.533 |
0.720 |
15 |
74720644 |
missense variant
|
T/A;C;G
|
snv |
0.11
|
5.9E-02
|
0.010 |
1.000 |
1 |
2006 |
2006 |
rs1052133
|
|
147
|
0.476 |
0.800 |
3 |
9757089 |
missense variant
|
C/G
|
snv |
0.27
|
0.22
|
0.010 |
1.000 |
1 |
1999 |
1999 |
rs1057519847
|
|
72
|
0.570 |
0.560 |
7 |
55191821 |
missense variant
|
CT/AG
|
mnv |
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1057519848
|
|
72
|
0.570 |
0.560 |
7 |
55191822 |
missense variant
|
TG/GT
|
mnv |
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1057520001
|
|
23
|
0.677 |
0.360 |
17 |
7674886 |
missense variant
|
A/C;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs1060501327
|
|
4
|
0.851 |
0.080 |
1 |
45332251 |
missense variant
|
A/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs10845498
|
|
2
|
0.925 |
0.080 |
12 |
12241640 |
intron variant
|
G/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs10849605
|
|
4
|
0.882 |
0.080 |
12 |
955272 |
intron variant
|
T/C
|
snv |
|
0.49
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1131691014
|
|
214
|
0.439 |
0.800 |
17 |
7676154 |
frameshift variant
|
-/C
|
ins |
|
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs121434568
|
|
73
|
0.568 |
0.560 |
7 |
55191822 |
missense variant
|
T/A;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs121434592
|
|
54
|
0.595 |
0.640 |
14 |
104780214 |
missense variant
|
C/T
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs121913376
|
|
2
|
0.925 |
0.080 |
7 |
140781597 |
missense variant
|
C/A;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs1367644026
|
|
5
|
0.925 |
0.080 |
12 |
52520259 |
missense variant
|
C/A;T
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs16901904
|
|
7
|
0.790 |
0.160 |
8 |
127015257 |
intron variant
|
T/C
|
snv |
|
0.27
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1801270
|
|
22
|
0.689 |
0.400 |
6 |
36684194 |
missense variant
|
C/A;T
|
snv |
0.15;
4.4E-05
|
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs201701502
|
|
5
|
0.851 |
0.080 |
1 |
162775837 |
missense variant
|
C/G;T
|
snv |
1.5E-04
|
2.1E-05
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs2070600
|
|
82
|
0.561 |
0.760 |
6 |
32183666 |
missense variant
|
C/T
|
snv |
5.3E-02
|
3.6E-02
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs2151280
|
|
16
|
0.701 |
0.360 |
9 |
22034720 |
non coding transcript exon variant
|
G/A
|
snv |
|
0.46
|
0.010 |
< 0.001 |
1 |
2019 |
2019 |
rs2233947
|
|
6
|
0.851 |
0.080 |
6 |
31139278 |
non coding transcript exon variant
|
C/T
|
snv |
|
9.3E-03
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs2239895
|
|
2
|
0.925 |
0.080 |
11 |
65423976 |
non coding transcript exon variant
|
G/C
|
snv |
|
3.9E-02
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs2835267
|
|
6
|
0.827 |
0.080 |
21 |
36074727 |
intron variant
|
T/C
|
snv |
|
0.63
|
0.010 |
< 0.001 |
1 |
2017 |
2017 |
rs3787728
|
|
5
|
0.851 |
0.080 |
21 |
36071595 |
intron variant
|
T/C
|
snv |
|
0.74
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs401681
|
|
42
|
0.620 |
0.640 |
5 |
1321972 |
intron variant
|
C/T
|
snv |
|
0.48
|
0.010 |
1.000 |
1 |
2014 |
2014 |