rs10030601
|
|
1
|
1.000 |
0.040 |
4 |
149804060 |
intron variant
|
T/C
|
snv |
|
0.22
|
0.800 |
1.000 |
1 |
2012 |
2012 |
rs10157763
|
|
2
|
1.000 |
0.040 |
1 |
243831739 |
intron variant
|
T/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs10234411
|
|
1
|
1.000 |
0.040 |
7 |
87535576 |
intron variant
|
T/A;C;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1024611
|
|
63
|
0.568 |
0.800 |
17 |
34252769 |
upstream gene variant
|
A/G
|
snv |
|
0.28
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1045642
|
|
214
|
0.456 |
0.840 |
7 |
87509329 |
synonymous variant
|
A/G;T
|
snv |
0.50
|
|
0.100 |
0.750 |
32 |
2005 |
2018 |
rs1047891
|
|
34
|
0.827 |
0.200 |
2 |
210675783 |
missense variant
|
C/A
|
snv |
0.30
|
0.33
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs104894358
|
|
3
|
0.882 |
0.120 |
12 |
4912627 |
stop gained
|
C/G;T
|
snv |
4.0E-06
|
|
0.010 |
< 0.001 |
1 |
2010 |
2010 |
rs10496964
|
|
2
|
0.925 |
0.040 |
2 |
144602342 |
intergenic variant
|
C/T
|
snv |
|
0.12
|
0.800 |
1.000 |
1 |
2012 |
2012 |
rs1051740
|
|
56
|
0.592 |
0.760 |
1 |
225831932 |
missense variant
|
T/C
|
snv |
0.32
|
0.27
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1057516064
|
|
3
|
0.925 |
0.120 |
MT |
9237 |
missense variant
|
G/A
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs1057516085
|
|
8
|
0.827 |
0.080 |
20 |
63444747 |
missense variant
|
C/T
|
snv |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1057518801
|
|
5
|
0.851 |
0.080 |
2 |
165130238 |
missense variant
|
A/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs1057518988
|
|
3
|
0.925 |
0.040 |
12 |
13571859 |
missense variant
|
T/C
|
snv |
|
|
0.700 |
|
0 |
|
|
rs1057520918
|
|
11
|
0.790 |
0.160 |
19 |
13262780 |
missense variant
|
C/T
|
snv |
|
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs1057910
|
|
12
|
0.776 |
0.280 |
10 |
94981296 |
missense variant
|
A/C;G
|
snv |
6.3E-02;
4.0E-06
|
|
0.010 |
1.000 |
1 |
1998 |
1998 |
rs1064797102
|
|
15
|
0.827 |
0.120 |
8 |
91071136 |
splice acceptor variant
|
A/G
|
snv |
|
|
0.700 |
|
0 |
|
|
rs1064797103
|
|
9
|
0.827 |
0.280 |
8 |
91078597 |
missense variant
|
A/G
|
snv |
|
|
0.700 |
|
0 |
|
|
rs10818488
|
|
8
|
0.776 |
0.360 |
9 |
120942809 |
regulatory region variant
|
A/G
|
snv |
|
0.51
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs10868235
|
|
6
|
0.925 |
0.040 |
9 |
84878840 |
intron variant
|
C/T
|
snv |
|
0.40
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1105879
|
|
11
|
0.790 |
0.240 |
2 |
233693556 |
missense variant
|
A/C
|
snv |
0.35
|
0.34
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1109771
|
|
1
|
1.000 |
0.040 |
6 |
32219828 |
intron variant
|
A/G
|
snv |
0.57
|
0.54
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs111577701
|
|
1
|
1.000 |
0.040 |
3 |
168143620 |
intergenic variant
|
C/T
|
snv |
|
0.13
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs111908689
|
|
1
|
1.000 |
0.040 |
11 |
85938055 |
downstream gene variant
|
C/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs11214136
|
|
1
|
1.000 |
0.040 |
11 |
112211286 |
intron variant
|
T/C
|
snv |
|
0.12
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs1128503
|
|
64
|
0.564 |
0.760 |
7 |
87550285 |
synonymous variant
|
A/G
|
snv |
0.54
|
0.63
|
0.030 |
0.667 |
3 |
2009 |
2011 |