rs10993994
|
|
15
|
0.763 |
0.280 |
10 |
46046326 |
5 prime UTR variant
|
A/G
|
snv |
|
0.54
|
0.800 |
1.000 |
30 |
2008 |
2019 |
rs4430796
|
|
14
|
0.790 |
0.280 |
17 |
37738049 |
intron variant
|
A/G
|
snv |
|
0.52
|
0.800 |
1.000 |
18 |
2008 |
2018 |
rs137852578
|
|
10
|
0.827 |
0.080 |
X |
67723710 |
missense variant
|
A/G
|
snv |
|
|
0.800 |
1.000 |
14 |
2002 |
2015 |
rs4792311
|
|
9
|
0.776 |
0.160 |
17 |
13011692 |
missense variant
|
G/A;C
|
snv |
0.27
|
|
0.090 |
1.000 |
9 |
2002 |
2010 |
rs6983561
|
|
3
|
0.925 |
0.080 |
8 |
127094635 |
intron variant
|
A/C
|
snv |
|
0.17
|
0.780 |
1.000 |
9 |
2008 |
2017 |
rs4242382
|
|
9
|
0.763 |
0.240 |
8 |
127505328 |
intergenic variant
|
A/G;T
|
snv |
|
|
0.740 |
1.000 |
8 |
2008 |
2015 |
rs7501939
|
|
12
|
0.776 |
0.280 |
17 |
37741165 |
intron variant
|
C/T
|
snv |
|
0.41
|
0.740 |
1.000 |
8 |
2008 |
2018 |
rs10090154
|
|
7
|
0.807 |
0.160 |
8 |
127519892 |
intergenic variant
|
T/A;C
|
snv |
|
|
0.070 |
1.000 |
7 |
2008 |
2017 |
rs12653946
|
|
5
|
0.882 |
0.080 |
5 |
1895715 |
intron variant
|
C/T
|
snv |
|
0.43
|
0.740 |
1.000 |
7 |
2010 |
2013 |
rs7837688
|
|
2
|
0.925 |
0.080 |
8 |
127527115 |
intergenic variant
|
T/G
|
snv |
|
0.91
|
0.710 |
1.000 |
7 |
2007 |
2013 |
rs1456315
|
|
9
|
0.790 |
0.200 |
8 |
127091692 |
non coding transcript exon variant
|
T/A;C
|
snv |
|
|
0.720 |
1.000 |
6 |
2010 |
2014 |
rs3787016
|
|
24
|
0.677 |
0.280 |
19 |
1090804 |
intron variant
|
A/G
|
snv |
|
0.78
|
0.060 |
1.000 |
6 |
2011 |
2019 |
rs41341748
|
|
6
|
0.827 |
0.120 |
8 |
16155085 |
stop gained
|
G/A;C
|
snv |
8.3E-03;
2.8E-05
|
|
0.060 |
1.000 |
6 |
2004 |
2006 |
rs4242384
|
|
3
|
0.882 |
0.160 |
8 |
127506309 |
regulatory region variant
|
C/A
|
snv |
|
0.88
|
0.700 |
1.000 |
6 |
2008 |
2013 |
rs1048943
|
|
88
|
0.533 |
0.720 |
15 |
74720644 |
missense variant
|
T/A;C;G
|
snv |
0.11
|
5.9E-02
|
0.050 |
1.000 |
5 |
2005 |
2019 |
rs10896449
|
|
7
|
0.827 |
0.200 |
11 |
69227200 |
intergenic variant
|
A/G
|
snv |
|
0.53
|
0.720 |
1.000 |
5 |
2008 |
2013 |
rs137852603
|
|
1
|
1.000 |
0.080 |
10 |
110280017 |
missense variant
|
A/C
|
snv |
|
|
0.800 |
1.000 |
5 |
2008 |
2015 |
rs16901966
|
|
3
|
0.925 |
0.080 |
8 |
127098007 |
intron variant
|
A/G
|
snv |
|
0.13
|
0.730 |
1.000 |
5 |
2008 |
2016 |
rs1805087
|
|
135
|
0.496 |
0.800 |
1 |
236885200 |
missense variant
|
A/G
|
snv |
0.20
|
0.21
|
0.050 |
1.000 |
5 |
2010 |
2018 |
rs587780194
|
|
1
|
1.000 |
0.080 |
22 |
28699866 |
missense variant
|
T/A;C
|
snv |
1.6E-05
|
|
0.700 |
1.000 |
5 |
2008 |
2015 |
rs750984976
|
|
1
|
1.000 |
0.080 |
22 |
28699879 |
missense variant
|
T/C;G
|
snv |
4.0E-06
|
|
0.700 |
1.000 |
5 |
2008 |
2015 |
rs77130927
|
|
3
|
0.882 |
0.120 |
22 |
28725031 |
missense variant
|
G/A
|
snv |
1.0E-03
|
5.5E-04
|
0.700 |
1.000 |
5 |
2008 |
2015 |
rs1016343
|
|
8
|
0.807 |
0.240 |
8 |
127081052 |
non coding transcript exon variant
|
C/T
|
snv |
|
0.20
|
0.700 |
1.000 |
4 |
2008 |
2013 |
rs1050450
|
|
43
|
0.623 |
0.600 |
3 |
49357401 |
missense variant
|
G/A
|
snv |
0.28
|
0.30
|
0.040 |
1.000 |
4 |
2007 |
2014 |
rs11549467
|
|
30
|
0.653 |
0.400 |
14 |
61740857 |
missense variant
|
G/A
|
snv |
8.9E-03
|
7.0E-03
|
0.040 |
1.000 |
4 |
2007 |
2013 |