rs11994014
|
|
5
|
0.827 |
0.200 |
8 |
24944767 |
intergenic variant
|
A/G
|
snv |
|
0.70
|
0.020 |
1.000 |
2 |
2014 |
2018 |
rs1217691063
|
|
614
|
0.330 |
0.920 |
1 |
11796309 |
missense variant
|
A/G
|
snv |
4.0E-06
|
7.0E-06
|
0.020 |
1.000 |
2 |
2014 |
2015 |
rs1424266770
|
|
10
|
0.790 |
0.200 |
4 |
184632307 |
missense variant
|
C/G
|
snv |
8.0E-06
|
|
0.020 |
1.000 |
2 |
2010 |
2014 |
rs1475170339
|
|
18
|
0.732 |
0.240 |
16 |
1792325 |
missense variant
|
T/C;G
|
snv |
|
|
0.020 |
1.000 |
2 |
2005 |
2007 |
rs17489363
|
|
3
|
0.882 |
0.080 |
2 |
214809617 |
5 prime UTR variant
|
A/G
|
snv |
0.73
|
0.74
|
0.020 |
1.000 |
2 |
2018 |
2019 |
rs1800562
|
|
262
|
0.435 |
0.880 |
6 |
26092913 |
missense variant
|
G/A
|
snv |
3.3E-02
|
3.8E-02
|
0.020 |
1.000 |
2 |
2011 |
2014 |
rs201216664
|
|
5
|
0.851 |
0.080 |
17 |
51171503 |
missense variant
|
A/G
|
snv |
|
|
0.020 |
1.000 |
2 |
1995 |
1999 |
rs217727
|
|
34
|
0.641 |
0.480 |
11 |
1995678 |
non coding transcript exon variant
|
G/A
|
snv |
0.20
|
|
0.020 |
0.500 |
2 |
2019 |
2019 |
rs221634
|
|
4
|
0.851 |
0.080 |
6 |
105080213 |
3 prime UTR variant
|
T/A
|
snv |
|
0.52
|
0.020 |
1.000 |
2 |
2016 |
2017 |
rs2839698
|
|
25
|
0.662 |
0.520 |
11 |
1997623 |
non coding transcript exon variant
|
G/A
|
snv |
0.41
|
|
0.020 |
0.500 |
2 |
2019 |
2019 |
rs3024270
|
|
8
|
0.776 |
0.200 |
11 |
1996209 |
non coding transcript exon variant
|
C/G;T
|
snv |
0.46;
5.2E-06
|
|
0.020 |
0.500 |
2 |
2019 |
2019 |
rs34637584
|
|
78
|
0.583 |
0.480 |
12 |
40340400 |
missense variant
|
G/A
|
snv |
5.3E-04
|
3.6E-04
|
0.020 |
1.000 |
2 |
2012 |
2018 |
rs368087026
|
|
33
|
0.637 |
0.520 |
21 |
45530890 |
missense variant
|
G/A
|
snv |
|
|
0.020 |
1.000 |
2 |
2014 |
2015 |
rs3768716
|
|
4
|
0.851 |
0.080 |
2 |
214771070 |
intron variant
|
T/C
|
snv |
|
0.16
|
0.020 |
1.000 |
2 |
2016 |
2019 |
rs4938723
|
|
60
|
0.574 |
0.680 |
11 |
111511840 |
intron variant
|
T/C
|
snv |
|
0.32
|
0.020 |
1.000 |
2 |
2019 |
2019 |
rs63751163
|
|
7
|
0.807 |
0.120 |
14 |
73192844 |
missense variant
|
T/C
|
snv |
|
|
0.020 |
1.000 |
2 |
2000 |
2001 |
rs63751273
|
|
42
|
0.645 |
0.280 |
17 |
46010389 |
missense variant
|
C/T
|
snv |
|
|
0.020 |
1.000 |
2 |
2016 |
2019 |
rs6441201
|
|
3
|
0.882 |
0.080 |
3 |
158460535 |
intron variant
|
G/A
|
snv |
|
0.51
|
0.020 |
1.000 |
2 |
2017 |
2018 |
rs74315406
|
|
5
|
0.851 |
0.160 |
20 |
4699870 |
missense variant
|
A/G
|
snv |
|
|
0.020 |
1.000 |
2 |
1997 |
2000 |
rs775144154
|
|
38
|
0.627 |
0.600 |
21 |
45531904 |
missense variant
|
C/A;T
|
snv |
9.7E-06;
1.4E-05
|
|
0.020 |
1.000 |
2 |
2014 |
2015 |
rs863225285
|
|
5
|
0.851 |
0.080 |
2 |
29209789 |
missense variant
|
T/G
|
snv |
|
|
0.020 |
1.000 |
2 |
2017 |
2018 |
rs10055201
|
|
3
|
0.882 |
0.080 |
5 |
55865274 |
intron variant
|
A/G
|
snv |
|
0.76
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1024611
|
|
63
|
0.568 |
0.800 |
17 |
34252769 |
upstream gene variant
|
A/G
|
snv |
|
0.28
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1027702
|
|
3
|
0.882 |
0.080 |
1 |
161743067 |
intergenic variant
|
C/T
|
snv |
|
0.51
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1039659576
|
|
21
|
0.689 |
0.520 |
1 |
236803473 |
missense variant
|
A/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |