rs3923809
|
|
1
|
1.000 |
0.080 |
6 |
38473194 |
intron variant
|
A/G
|
snv |
|
0.32
|
0.820 |
1.000 |
4 |
2007 |
2017 |
rs1026732
|
|
1
|
1.000 |
0.080 |
15 |
67802747 |
intron variant
|
G/A
|
snv |
|
0.38
|
0.720 |
1.000 |
3 |
2007 |
2018 |
rs1975197
|
|
1
|
1.000 |
0.080 |
9 |
8846955 |
intron variant
|
G/A
|
snv |
|
0.16
|
0.810 |
1.000 |
3 |
2008 |
2011 |
rs4626664
|
|
1
|
1.000 |
0.080 |
9 |
9261737 |
intron variant
|
G/A
|
snv |
|
0.20
|
0.820 |
1.000 |
3 |
2008 |
2014 |
rs11635424
|
|
1
|
1.000 |
0.080 |
15 |
67745240 |
intron variant
|
A/G
|
snv |
|
0.53
|
0.710 |
1.000 |
2 |
2007 |
2018 |
rs3784709
|
|
1
|
1.000 |
0.080 |
15 |
67779937 |
intron variant
|
C/T
|
snv |
|
0.36
|
0.710 |
1.000 |
2 |
2007 |
2018 |
rs4489954
|
|
1
|
1.000 |
0.080 |
15 |
67779737 |
intron variant
|
T/A;G
|
snv |
|
|
0.710 |
1.000 |
2 |
2007 |
2018 |
rs6494696
|
|
1
|
1.000 |
0.080 |
15 |
67810868 |
downstream gene variant
|
G/A;C
|
snv |
|
|
0.710 |
1.000 |
2 |
2007 |
2017 |
rs10208712
|
|
1
|
1.000 |
0.080 |
2 |
3986856 |
regulatory region variant
|
A/G
|
snv |
|
0.26
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs10952927
|
|
1
|
1.000 |
0.080 |
7 |
88729746 |
intron variant
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs111652004
|
|
1
|
1.000 |
0.080 |
15 |
47068169 |
intergenic variant
|
G/T
|
snv |
|
8.6E-02
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs12046503
|
|
1
|
1.000 |
0.080 |
1 |
106652717 |
intergenic variant
|
T/C
|
snv |
|
0.32
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs12450895
|
|
1
|
1.000 |
0.080 |
17 |
48695414 |
intron variant
|
G/A
|
snv |
|
0.27
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs12962305
|
|
1
|
1.000 |
0.080 |
18 |
44290278 |
intron variant
|
C/T
|
snv |
|
0.21
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs138915427
|
|
1
|
1.000 |
0.080 |
9 |
8341723 |
missense variant
|
C/A;G;T
|
snv |
4.0E-06;
2.0E-05;
2.4E-05
|
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs17636328
|
|
1
|
1.000 |
0.080 |
6 |
37522755 |
intron variant
|
A/G
|
snv |
|
0.14
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs1800652
|
|
1
|
1.000 |
0.080 |
9 |
69046200 |
intron variant
|
G/A
|
snv |
|
0.24
|
0.010 |
< 0.001 |
1 |
2013 |
2013 |
rs1820989
|
|
1
|
1.000 |
0.080 |
2 |
67842758 |
intergenic variant
|
A/C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs1836229
|
|
1
|
1.000 |
0.080 |
9 |
8820573 |
intron variant
|
A/C;G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs1848460
|
|
1
|
1.000 |
0.080 |
3 |
3406460 |
intron variant
|
A/T
|
snv |
|
0.33
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs1918752
|
|
1
|
1.000 |
0.080 |
6 |
144587941 |
intron variant
|
A/T
|
snv |
|
0.22
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1983167
|
|
1
|
1.000 |
0.080 |
X |
42989135 |
regulatory region variant
|
T/C
|
snv |
|
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs2229940
|
|
1
|
1.000 |
0.080 |
4 |
46993349 |
missense variant
|
G/T
|
snv |
0.32
|
0.31
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs340561
|
|
1
|
1.000 |
0.080 |
13 |
72274018 |
intergenic variant
|
G/T
|
snv |
|
0.23
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs35041767
|
|
1
|
1.000 |
0.080 |
9 |
9261737 |
intron variant
|
-/C
|
ins |
|
|
0.700 |
1.000 |
1 |
2008 |
2008 |