rs10255208
|
|
2
|
0.925 |
0.160 |
7 |
36819038 |
non coding transcript exon variant
|
A/G
|
snv |
|
0.46
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1049353
|
|
42
|
0.630 |
0.600 |
6 |
88143916 |
synonymous variant
|
C/T
|
snv |
0.21
|
0.20
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1056534
|
|
5
|
0.882 |
0.200 |
17 |
82750725 |
synonymous variant
|
C/A;G;T
|
snv |
0.62
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1063537
|
|
6
|
0.807 |
0.320 |
3 |
186856286 |
3 prime UTR variant
|
C/T
|
snv |
|
9.6E-02
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs10770125
|
|
4
|
0.882 |
0.200 |
11 |
2147784 |
missense variant
|
A/G
|
snv |
0.49
|
0.40
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs10811661
|
|
22
|
0.724 |
0.400 |
9 |
22134095 |
intergenic variant
|
T/C
|
snv |
|
0.14
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs10951509
|
|
1
|
1.000 |
0.120 |
7 |
37173878 |
intron variant
|
G/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs11130362
|
|
1
|
1.000 |
0.120 |
3 |
53231750 |
non coding transcript exon variant
|
C/T
|
snv |
|
0.24
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1129456
|
|
1
|
1.000 |
0.120 |
15 |
32734466 |
3 prime UTR variant
|
A/T
|
snv |
|
0.19
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs1136410
|
|
70
|
0.559 |
0.760 |
1 |
226367601 |
missense variant
|
A/G
|
snv |
0.21
|
0.15
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1137933
|
|
4
|
0.882 |
0.160 |
17 |
27778906 |
synonymous variant
|
G/A
|
snv |
0.20
|
0.21
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs1143770
|
|
4
|
0.882 |
0.200 |
11 |
122146890 |
intron variant
|
C/T
|
snv |
|
0.53
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs11538209
|
|
2
|
1.000 |
0.120 |
4 |
73404356 |
missense variant
|
T/C
|
snv |
|
|
0.010 |
< 0.001 |
1 |
2001 |
2001 |
rs1157043147
|
|
1
|
1.000 |
0.120 |
17 |
63477150 |
missense variant
|
T/C
|
snv |
|
2.8E-05
|
0.010 |
1.000 |
1 |
2003 |
2003 |
rs11645214
|
|
1
|
1.000 |
0.120 |
16 |
70575084 |
3 prime UTR variant
|
A/G
|
snv |
|
0.39
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs11646213
|
|
6
|
0.827 |
0.320 |
16 |
82609046 |
intergenic variant
|
A/T
|
snv |
|
0.47
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs11651270
|
|
4
|
0.882 |
0.240 |
17 |
5521757 |
missense variant
|
T/C
|
snv |
0.45
|
0.47
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs11771443
|
|
8
|
0.790 |
0.360 |
7 |
150990599 |
upstream gene variant
|
C/T
|
snv |
|
0.16
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs1177506410
|
|
12
|
0.776 |
0.240 |
1 |
230706148 |
missense variant
|
G/C
|
snv |
4.0E-06
|
7.0E-06
|
0.010 |
1.000 |
1 |
2004 |
2004 |
rs11886047
|
|
1
|
1.000 |
0.120 |
2 |
43623451 |
upstream gene variant
|
T/A;C
|
snv |
|
0.20
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs11887534
|
|
29
|
0.653 |
0.440 |
2 |
43839108 |
missense variant
|
G/A;C
|
snv |
6.4E-06;
6.7E-02
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs11915160
|
|
5
|
0.851 |
0.200 |
3 |
181713783 |
3 prime UTR variant
|
C/A
|
snv |
|
0.11
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs12449782
|
|
3
|
0.925 |
0.200 |
17 |
63498888 |
intron variant
|
G/A
|
snv |
|
0.41
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs1252906
|
|
1
|
1.000 |
0.120 |
14 |
59192073 |
intron variant
|
A/C;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1253192
|
|
1
|
1.000 |
0.120 |
14 |
59376688 |
intergenic variant
|
A/G
|
snv |
|
0.92
|
0.010 |
1.000 |
1 |
2013 |
2013 |