rs3761548
|
|
42
|
0.620 |
0.680 |
X |
49261784 |
intron variant
|
G/A;T
|
snv |
|
|
0.020 |
1.000 |
2 |
2013 |
2013 |
rs397507444
|
|
306
|
0.405 |
0.880 |
1 |
11794407 |
missense variant
|
T/G
|
snv |
|
|
0.020 |
1.000 |
2 |
2012 |
2020 |
rs10249788
|
|
6
|
0.827 |
0.160 |
7 |
17298523 |
intron variant
|
C/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs1043210477
|
|
19
|
0.701 |
0.520 |
3 |
49358250 |
missense variant
|
G/A
|
snv |
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs1130409
|
|
72
|
0.555 |
0.720 |
14 |
20456995 |
missense variant
|
T/A;C;G
|
snv |
4.0E-06;
4.0E-06;
0.42
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1141718
|
|
15
|
0.724 |
0.280 |
6 |
159688224 |
missense variant
|
A/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs11575993
|
|
2
|
0.925 |
0.040 |
6 |
159688219 |
missense variant
|
G/A
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs11940117
|
|
2
|
0.925 |
0.040 |
4 |
10725083 |
intergenic variant
|
C/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1237063529
|
|
13
|
0.752 |
0.360 |
21 |
43058894 |
missense variant
|
T/G
|
snv |
5.6E-06
|
|
0.010 |
1.000 |
1 |
2020 |
2020 |
rs13208776
|
|
3
|
0.882 |
0.040 |
6 |
168540944 |
intron variant
|
G/A;C
|
snv |
|
|
0.010 |
< 0.001 |
1 |
2011 |
2011 |
rs1417210
|
|
2
|
0.925 |
0.040 |
10 |
71376162 |
intron variant
|
G/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1464510
|
|
9
|
0.807 |
0.280 |
3 |
188394766 |
intron variant
|
C/A;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1534284
|
|
2
|
0.925 |
0.040 |
12 |
53299748 |
missense variant
|
A/G;T
|
snv |
0.99;
4.0E-06
|
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs16139
|
|
36
|
0.658 |
0.560 |
7 |
24285260 |
missense variant
|
T/A;C
|
snv |
4.0E-06;
3.0E-02
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs17587
|
|
8
|
0.807 |
0.280 |
6 |
32857313 |
missense variant
|
G/A;T
|
snv |
0.24;
4.1E-06;
4.1E-06
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs2232365
|
|
16
|
0.716 |
0.480 |
X |
49259429 |
intron variant
|
T/C
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs2234663
|
|
14
|
0.716 |
0.480 |
2 |
113130529 |
intron variant
|
ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC/-;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC
|
delins |
|
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs2294020
|
|
10
|
0.763 |
0.280 |
X |
49246763 |
missense variant
|
A/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs231775
|
|
115
|
0.504 |
0.720 |
2 |
203867991 |
missense variant
|
A/G;T
|
snv |
0.42;
4.0E-06
|
|
0.010 |
< 0.001 |
1 |
2009 |
2009 |
rs2456973
|
|
4
|
0.925 |
0.040 |
12 |
56023144 |
intron variant
|
A/C;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs4744411
|
|
3
|
0.925 |
0.040 |
9 |
94926763 |
intron variant
|
G/A;C;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs4946936
|
|
8
|
0.790 |
0.160 |
6 |
108682118 |
3 prime UTR variant
|
T/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs4986790
|
|
223
|
0.438 |
0.800 |
9 |
117713024 |
missense variant
|
A/G;T
|
snv |
6.1E-02;
4.0E-06
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs5742905
|
|
22
|
0.701 |
0.360 |
21 |
43063074 |
missense variant
|
A/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs59374417
|
|
2
|
0.925 |
0.040 |
3 |
119569567 |
intergenic variant
|
A/C;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |