rs9981660
|
|
3
|
0.882 |
0.080 |
21 |
42317828 |
upstream gene variant
|
G/A
|
snv |
|
0.11
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs9471643
|
|
6
|
0.882 |
0.080 |
6 |
41751177 |
intron variant
|
G/C
|
snv |
|
0.19
|
0.020 |
1.000 |
2 |
2014 |
2016 |
rs9315542
|
|
1
|
1.000 |
0.040 |
13 |
38057334 |
intron variant
|
T/C
|
snv |
|
0.26
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs917997
|
|
20
|
0.701 |
0.480 |
2 |
102454108 |
downstream gene variant
|
T/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs895819
|
|
46
|
0.623 |
0.560 |
19 |
13836478 |
non coding transcript exon variant
|
T/A;C;G
|
snv |
0.34
|
0.38
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs873601
|
|
25
|
0.677 |
0.360 |
13 |
102875987 |
3 prime UTR variant
|
G/A
|
snv |
|
0.59
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs830083
|
|
6
|
0.807 |
0.120 |
11 |
47232500 |
intron variant
|
G/A;C;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs8111742
|
|
4
|
0.851 |
0.120 |
19 |
51692221 |
intron variant
|
G/A;C
|
snv |
|
0.30
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs7749023
|
|
1
|
1.000 |
0.040 |
6 |
42093995 |
non coding transcript exon variant
|
A/C;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs7747696
|
|
1
|
1.000 |
0.040 |
6 |
42093217 |
non coding transcript exon variant
|
A/G
|
snv |
|
0.54
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs765803011
|
|
1
|
1.000 |
0.040 |
16 |
27363094 |
missense variant
|
C/G;T
|
snv |
4.0E-06;
1.6E-05
|
|
0.010 |
1.000 |
1 |
2006 |
2006 |
rs764097618
|
|
1
|
1.000 |
0.040 |
16 |
27360794 |
splice donor variant
|
G/A
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2006 |
2006 |
rs760805
|
|
9
|
0.776 |
0.240 |
1 |
24925432 |
intron variant
|
A/T
|
snv |
|
0.42
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs7521584
|
|
3
|
1.000 |
0.040 |
1 |
1168578 |
upstream gene variant
|
T/A;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs7481521
|
|
1
|
1.000 |
0.040 |
11 |
1027811 |
missense variant
|
C/T
|
snv |
0.50
|
0.47
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs6939861
|
|
3
|
0.882 |
0.080 |
6 |
41735303 |
intron variant
|
G/A
|
snv |
|
0.24
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs6912200
|
|
3
|
0.925 |
0.080 |
6 |
41750170 |
intron variant
|
C/T
|
snv |
|
0.54
|
0.010 |
< 0.001 |
1 |
2016 |
2016 |
rs6878265
|
|
2
|
1.000 |
0.040 |
5 |
120069960 |
intergenic variant
|
C/T
|
snv |
|
0.29
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs6672420
|
|
6
|
0.827 |
0.120 |
1 |
24964519 |
missense variant
|
A/T
|
snv |
0.56
|
0.50
|
0.010 |
< 0.001 |
1 |
2009 |
2009 |
rs6498486
|
|
8
|
0.776 |
0.200 |
16 |
13919809 |
upstream gene variant
|
A/C
|
snv |
|
0.27
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs6458238
|
|
4
|
0.882 |
0.080 |
6 |
41749967 |
intron variant
|
G/A;C
|
snv |
|
|
0.040 |
1.000 |
4 |
2013 |
2016 |
rs629367
|
|
11
|
0.776 |
0.200 |
11 |
122146306 |
intron variant
|
C/A
|
snv |
|
0.88
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs61516247
|
|
1
|
1.000 |
0.040 |
6 |
40344500 |
non coding transcript exon variant
|
G/A
|
snv |
|
0.17
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs4986791
|
|
182
|
0.456 |
0.840 |
9 |
117713324 |
missense variant
|
C/T
|
snv |
5.7E-02
|
4.9E-02
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs4833095
|
|
28
|
0.662 |
0.480 |
4 |
38798089 |
missense variant
|
T/C
|
snv |
0.38
|
0.44
|
0.010 |
1.000 |
1 |
2015 |
2015 |