rs113488022
|
|
490
|
0.351 |
0.840 |
7 |
140753336 |
missense variant
|
A/C;G;T
|
snv |
4.0E-06
|
|
0.100 |
1.000 |
12 |
2008 |
2019 |
rs231775
|
|
115
|
0.504 |
0.720 |
2 |
203867991 |
missense variant
|
A/G;T
|
snv |
0.42;
4.0E-06
|
|
0.090 |
1.000 |
9 |
2001 |
2019 |
rs2476601
|
|
121
|
0.498 |
0.800 |
1 |
113834946 |
missense variant
|
A/G
|
snv |
0.93
|
0.93
|
0.850 |
0.667 |
6 |
2006 |
2017 |
rs12976445
|
|
20
|
0.689 |
0.600 |
19 |
51693200 |
non coding transcript exon variant
|
T/C
|
snv |
|
0.45
|
0.020 |
1.000 |
2 |
2014 |
2017 |
rs28665122
|
|
7
|
0.807 |
0.240 |
15 |
101277522 |
upstream gene variant
|
C/T
|
snv |
|
0.24
|
0.020 |
1.000 |
2 |
2014 |
2015 |
rs4986790
|
|
223
|
0.438 |
0.800 |
9 |
117713024 |
missense variant
|
A/G;T
|
snv |
6.1E-02;
4.0E-06
|
|
0.020 |
0.500 |
2 |
2014 |
2020 |
rs4986791
|
|
182
|
0.456 |
0.840 |
9 |
117713324 |
missense variant
|
C/T
|
snv |
5.7E-02
|
4.9E-02
|
0.020 |
0.500 |
2 |
2014 |
2020 |
rs744166
|
|
22
|
0.689 |
0.560 |
17 |
42362183 |
intron variant
|
A/G
|
snv |
|
0.48
|
0.020 |
1.000 |
2 |
2014 |
2015 |
rs763780
|
|
87
|
0.531 |
0.720 |
6 |
52236941 |
missense variant
|
T/C
|
snv |
6.7E-02
|
6.6E-02
|
0.020 |
1.000 |
2 |
2012 |
2018 |
rs10004195
|
|
8
|
0.790 |
0.320 |
4 |
38783103 |
upstream gene variant
|
T/A
|
snv |
|
0.29
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1042522
|
|
242
|
0.426 |
0.800 |
17 |
7676154 |
missense variant
|
G/C;T
|
snv |
0.67
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1053005
|
|
10
|
0.763 |
0.360 |
17 |
42313892 |
3 prime UTR variant
|
T/C
|
snv |
|
0.25
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1059703
|
|
6
|
0.851 |
0.280 |
X |
154013378 |
missense variant
|
G/A
|
snv |
0.67
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1061501
|
|
4
|
0.851 |
0.200 |
11 |
614864 |
synonymous variant
|
C/T
|
snv |
0.83
|
0.85
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs10774625
|
|
13
|
0.763 |
0.320 |
12 |
111472415 |
intron variant
|
A/G
|
snv |
|
0.66
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs111033243
|
|
5
|
0.827 |
0.400 |
7 |
107689112 |
missense variant
|
T/C
|
snv |
6.1E-04
|
8.1E-04
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs1133076
|
|
2
|
0.925 |
0.080 |
8 |
133113438 |
missense variant
|
G/A
|
snv |
0.48
|
0.56
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs1143627
|
|
47
|
0.605 |
0.760 |
2 |
112836810 |
5 prime UTR variant
|
G/A
|
snv |
|
0.56
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs11568820
|
|
27
|
0.672 |
0.480 |
12 |
47908762 |
intron variant
|
C/T
|
snv |
|
0.38
|
0.010 |
< 0.001 |
1 |
2019 |
2019 |
rs11571297
|
|
3
|
0.882 |
0.120 |
2 |
203880280 |
regulatory region variant
|
T/C
|
snv |
|
0.44
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs11611206
|
|
4
|
0.851 |
0.200 |
12 |
68274666 |
intron variant
|
G/A
|
snv |
|
0.15
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs11675434
|
|
5
|
0.827 |
0.240 |
2 |
1404043 |
non coding transcript exon variant
|
C/T
|
snv |
|
0.39
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs1179251
|
|
14
|
0.763 |
0.320 |
12 |
68251271 |
intron variant
|
C/G
|
snv |
|
0.18
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs11935941
|
|
2
|
1.000 |
0.040 |
4 |
148731326 |
intron variant
|
A/C
|
snv |
|
0.31
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs12101255
|
|
2
|
0.925 |
0.120 |
14 |
80984708 |
intron variant
|
C/T
|
snv |
|
0.37
|
0.010 |
1.000 |
1 |
2012 |
2012 |