rs864622007
|
|
2
|
0.882 |
0.200 |
X |
67711621 |
missense variant
|
T/A
|
snv |
|
|
0.830 |
1.000 |
0 |
2002 |
2010 |
rs1447295
|
|
3
|
0.658 |
0.400 |
8 |
127472793 |
intron variant
|
A/C;T
|
snv |
|
|
0.800 |
0.917 |
8 |
2007 |
2018 |
rs137852603
|
|
1
|
1.000 |
0.080 |
10 |
110280017 |
missense variant
|
A/C
|
snv |
|
|
0.800 |
1.000 |
5 |
2008 |
2015 |
rs6983267
|
|
13
|
0.578 |
0.440 |
8 |
127401060 |
non coding transcript exon variant
|
G/T
|
snv |
|
0.37
|
0.800 |
0.857 |
5 |
2007 |
2017 |
rs10993994
|
|
7
|
0.763 |
0.280 |
10 |
46046326 |
5 prime UTR variant
|
A/G
|
snv |
|
0.54
|
0.800 |
1.000 |
4 |
2008 |
2019 |
rs16901979
|
|
3
|
0.724 |
0.480 |
8 |
127112671 |
intron variant
|
C/A
|
snv |
|
0.16
|
0.800 |
0.950 |
3 |
2007 |
2018 |
rs4430796
|
|
7
|
0.790 |
0.280 |
17 |
37738049 |
intron variant
|
A/G
|
snv |
|
0.52
|
0.800 |
1.000 |
2 |
2008 |
2018 |
rs2735839
|
|
4
|
0.827 |
0.160 |
19 |
50861367 |
upstream gene variant
|
A/C;G
|
snv |
|
|
0.800 |
0.923 |
1 |
2008 |
2019 |
rs137852564
|
|
5
|
0.827 |
0.240 |
X |
67722976 |
missense variant
|
G/A;T
|
snv |
|
|
0.800 |
|
0 |
|
|
rs137852578
|
|
2
|
0.827 |
0.080 |
X |
67723710 |
missense variant
|
A/G
|
snv |
|
|
0.800 |
1.000 |
0 |
2002 |
2015 |
rs138213197
|
|
8
|
0.701 |
0.240 |
17 |
48728343 |
missense variant
|
C/T
|
snv |
1.8E-03
|
1.6E-03
|
0.800 |
0.935 |
0 |
2012 |
2019 |
rs351855
|
|
4
|
0.597 |
0.560 |
5 |
177093242 |
missense variant
|
G/A
|
snv |
0.33
|
0.26
|
0.780 |
0.900 |
4 |
2005 |
2017 |
rs6983561
|
|
2
|
0.925 |
0.080 |
8 |
127094635 |
intron variant
|
A/C
|
snv |
|
0.17
|
0.780 |
1.000 |
1 |
2008 |
2017 |
rs1859962
|
|
3
|
0.882 |
0.160 |
17 |
71112612 |
intron variant
|
G/T
|
snv |
|
0.56
|
0.770 |
0.900 |
3 |
2008 |
2016 |
rs339331
|
|
2
|
0.882 |
0.080 |
6 |
116888889 |
intron variant
|
T/C
|
snv |
|
0.28
|
0.760 |
0.857 |
1 |
2010 |
2016 |
rs17632542
|
|
3
|
0.925 |
0.080 |
19 |
50858501 |
missense variant
|
T/C
|
snv |
5.5E-02
|
4.9E-02
|
0.750 |
0.667 |
1 |
2011 |
2015 |
rs4242382
|
|
3
|
0.763 |
0.240 |
8 |
127505328 |
intergenic variant
|
A/G;T
|
snv |
|
|
0.740 |
1.000 |
4 |
2008 |
2015 |
rs7501939
|
|
7
|
0.776 |
0.280 |
17 |
37741165 |
intron variant
|
C/T
|
snv |
|
0.41
|
0.740 |
1.000 |
4 |
2008 |
2018 |
rs12653946
|
|
2
|
0.882 |
0.080 |
5 |
1895715 |
intron variant
|
C/T
|
snv |
|
0.43
|
0.740 |
1.000 |
3 |
2010 |
2013 |
rs137852593
|
|
2
|
0.827 |
0.160 |
X |
67717484 |
missense variant
|
G/A;C;T
|
snv |
2.2E-05;
1.1E-05;
9.1E-04
|
|
0.740 |
1.000 |
0 |
2000 |
2004 |
rs16901966
|
|
1
|
0.925 |
0.080 |
8 |
127098007 |
intron variant
|
A/G
|
snv |
|
0.13
|
0.730 |
1.000 |
2 |
2008 |
2016 |
rs5945572
|
|
3
|
0.882 |
0.160 |
X |
51486831 |
downstream gene variant
|
A/G
|
snv |
|
|
0.730 |
1.000 |
2 |
2008 |
2010 |
rs103294
|
|
5
|
0.827 |
0.200 |
19 |
54293995 |
downstream gene variant
|
T/C
|
snv |
|
0.82
|
0.730 |
1.000 |
1 |
2012 |
2014 |
rs620861
|
|
2
|
0.925 |
0.080 |
8 |
127323428 |
intron variant
|
G/A
|
snv |
|
0.36
|
0.730 |
0.750 |
1 |
2008 |
2017 |
rs1456315
|
|
2
|
0.790 |
0.200 |
8 |
127091692 |
non coding transcript exon variant
|
T/A;C
|
snv |
|
|
0.720 |
1.000 |
4 |
2010 |
2014 |