rs1800629
|
|
169
|
0.472 |
0.920 |
6 |
31575254 |
upstream gene variant
|
G/A
|
snv |
0.12
|
0.14
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1800630
|
|
17
|
0.701 |
0.480 |
6 |
31574699 |
upstream gene variant
|
C/A
|
snv |
|
0.14
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1801131
|
|
93
|
0.535 |
0.840 |
1 |
11794419 |
missense variant
|
T/G
|
snv |
0.29
|
0.26
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1801133
|
|
174
|
0.472 |
0.880 |
1 |
11796321 |
missense variant
|
G/A
|
snv |
0.31
|
0.27
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs197388
|
|
2
|
0.925 |
0.040 |
1 |
111754860 |
non coding transcript exon variant
|
A/T
|
snv |
|
0.27
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs199746824
|
|
6
|
0.807 |
0.040 |
1 |
171652139 |
missense variant
|
C/G;T
|
snv |
4.0E-06;
1.6E-05
|
|
0.010 |
1.000 |
1 |
2001 |
2001 |
rs199752860
|
|
2
|
0.925 |
0.040 |
1 |
171652578 |
missense variant
|
C/G
|
snv |
6.9E-04
|
1.5E-04
|
0.010 |
1.000 |
1 |
2000 |
2000 |
rs200208925
|
|
2
|
0.925 |
0.040 |
1 |
171652454 |
missense variant
|
A/G
|
snv |
6.4E-05
|
2.1E-05
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs200547613
|
|
2
|
0.925 |
0.040 |
1 |
171638675 |
missense variant
|
C/T
|
snv |
4.8E-05
|
1.4E-05
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs200710076
|
|
2
|
0.925 |
0.040 |
10 |
13109198 |
missense variant
|
C/A;G;T
|
snv |
8.0E-06;
2.0E-05;
2.4E-05
|
|
0.010 |
1.000 |
1 |
2004 |
2004 |
rs2149356
|
|
14
|
0.742 |
0.360 |
9 |
117711921 |
intron variant
|
T/G
|
snv |
|
0.54
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs2157719
|
|
17
|
0.708 |
0.360 |
9 |
22033367 |
non coding transcript exon variant
|
C/T
|
snv |
|
0.71
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs2234926
|
|
3
|
0.882 |
0.040 |
1 |
171652385 |
missense variant
|
C/T
|
snv |
0.15
|
0.11
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs2234927
|
|
4
|
0.851 |
0.040 |
1 |
171638703 |
missense variant
|
G/A;C
|
snv |
4.0E-06;
7.6E-04
|
|
0.010 |
1.000 |
1 |
2000 |
2000 |
rs2567206
|
|
7
|
0.827 |
0.200 |
2 |
38076389 |
non coding transcript exon variant
|
G/A
|
snv |
|
0.23
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs267606929
|
|
5
|
0.827 |
0.120 |
10 |
13132098 |
missense variant
|
A/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs267607161
|
|
16
|
0.742 |
0.360 |
18 |
31598580 |
missense variant
|
G/T
|
snv |
4.0E-06
|
7.0E-06
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs284489
|
|
3
|
0.882 |
0.080 |
8 |
104945792 |
intron variant
|
A/G
|
snv |
|
0.45
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs28936700
|
|
9
|
0.776 |
0.120 |
2 |
38075207 |
missense variant
|
C/G;T
|
snv |
5.0E-06;
3.2E-04
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs35703638
|
|
1
|
1.000 |
0.040 |
5 |
111106140 |
missense variant
|
G/A
|
snv |
8.3E-03
|
4.1E-03
|
0.010 |
1.000 |
1 |
2005 |
2005 |
rs361525
|
|
62
|
0.562 |
0.760 |
6 |
31575324 |
upstream gene variant
|
G/A
|
snv |
|
4.6E-02
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs369115487
|
|
1
|
1.000 |
0.040 |
2 |
38075373 |
missense variant
|
T/C
|
snv |
1.6E-05
|
1.4E-05
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs372487178
|
|
2
|
0.925 |
0.040 |
11 |
62616748 |
missense variant
|
C/T
|
snv |
|
2.1E-05
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs3766355
|
|
3
|
0.882 |
0.040 |
1 |
78491756 |
intron variant
|
C/A;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs3858145
|
|
3
|
0.882 |
0.040 |
10 |
68252081 |
regulatory region variant
|
A/G
|
snv |
|
0.33
|
0.010 |
1.000 |
1 |
2012 |
2012 |