rs12203592
|
|
38
|
0.649 |
0.320 |
6 |
396321 |
intron variant
|
C/T
|
snv |
|
0.10
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs2066853
|
|
34
|
0.653 |
0.600 |
7 |
17339486 |
missense variant
|
G/A
|
snv |
0.15
|
0.22
|
0.010 |
1.000 |
1 |
2012 |
2012 |
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 |
rs1041981
|
|
25
|
0.667 |
0.520 |
6 |
31573007 |
missense variant
|
C/A
|
snv |
0.35
|
0.38
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1126809
|
|
29
|
0.683 |
0.320 |
11 |
89284793 |
missense variant
|
G/A
|
snv |
0.18
|
0.18
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs16147
|
|
18
|
0.695 |
0.400 |
7 |
24283791 |
upstream gene variant
|
T/C
|
snv |
|
0.48
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs72928038
|
|
19
|
0.695 |
0.360 |
6 |
90267049 |
intron variant
|
G/A
|
snv |
|
0.11
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1043210477
|
|
19
|
0.701 |
0.520 |
3 |
49358250 |
missense variant
|
G/A
|
snv |
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs5742905
|
|
22
|
0.701 |
0.360 |
21 |
43063074 |
missense variant
|
A/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1202989817
|
|
18
|
0.716 |
0.360 |
21 |
31659813 |
missense variant
|
T/C;G
|
snv |
8.0E-06
|
7.0E-06
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1861494
|
|
15
|
0.716 |
0.400 |
12 |
68157629 |
intron variant
|
C/T
|
snv |
|
0.75
|
0.010 |
1.000 |
1 |
2017 |
2017 |
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 |
rs2111485
|
|
17
|
0.724 |
0.280 |
2 |
162254026 |
regulatory region variant
|
A/G
|
snv |
|
0.46
|
0.800 |
1.000 |
2 |
2012 |
2016 |
rs1141718
|
|
15
|
0.724 |
0.280 |
6 |
159688224 |
missense variant
|
A/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs12150220
|
|
14
|
0.724 |
0.360 |
17 |
5582047 |
missense variant
|
A/T
|
snv |
0.37
|
0.33
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs2395185
|
|
17
|
0.724 |
0.360 |
6 |
32465390 |
intron variant
|
G/T
|
snv |
|
0.29
|
0.700 |
1.000 |
1 |
2010 |
2010 |
rs1805008
|
|
16
|
0.732 |
0.240 |
16 |
89919736 |
missense variant
|
C/T
|
snv |
4.7E-02
|
4.8E-02
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs2516049
|
|
12
|
0.742 |
0.400 |
6 |
32602623 |
intergenic variant
|
T/C
|
snv |
|
0.27
|
0.700 |
1.000 |
1 |
2010 |
2010 |
rs769217
|
|
12
|
0.742 |
0.440 |
11 |
34461361 |
synonymous variant
|
C/T
|
snv |
0.25
|
0.22
|
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 |
rs4409785
|
|
12
|
0.752 |
0.240 |
11 |
95578258 |
intron variant
|
T/C
|
snv |
|
0.13
|
0.800 |
1.000 |
1 |
2012 |
2012 |
rs2294020
|
|
10
|
0.763 |
0.280 |
X |
49246763 |
missense variant
|
A/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs876657421
|
|
11
|
0.763 |
0.240 |
21 |
43063074 |
coding sequence variant
|
-/CCCAGCAAAAGCCCCACCTGGATGATCCACCCCAGTGATCTGCAGAGGGCGCGGCTTCAGGGCTCAAG;CCCAGCAAAAGCCCCACCTGGGTGATCCACCCCAGTGATCTGCAGAGGGCGCGGCTTCAGGGCTCAAG
|
delins |
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs12153855
|
|
11
|
0.776 |
0.320 |
6 |
32107027 |
intron variant
|
T/C
|
snv |
|
0.11
|
0.700 |
1.000 |
1 |
2010 |
2010 |