rs6983267
|
|
11
|
0.578 |
0.440 |
8 |
127401060 |
non coding transcript exon variant
|
G/T
|
snv |
|
0.37
|
0.700 |
1.000 |
14 |
2007 |
2019 |
rs3802842
|
|
9
|
0.695 |
0.280 |
11 |
111300984 |
intron variant
|
C/A
|
snv |
|
0.71
|
0.700 |
1.000 |
8 |
2008 |
2019 |
rs4939827
|
|
10
|
0.708 |
0.160 |
18 |
48927093 |
intron variant
|
T/A;C
|
snv |
|
|
0.700 |
1.000 |
8 |
2007 |
2019 |
rs16892766
|
|
10
|
0.716 |
0.240 |
8 |
116618444 |
intergenic variant
|
A/C
|
snv |
|
9.3E-02
|
0.700 |
1.000 |
6 |
2008 |
2019 |
rs704017
|
|
10
|
0.776 |
0.080 |
10 |
79059375 |
intron variant
|
A/G
|
snv |
|
0.55
|
0.700 |
1.000 |
6 |
2014 |
2019 |
rs11255841
|
|
10
|
0.776 |
0.080 |
10 |
8697617 |
intergenic variant
|
T/A
|
snv |
|
0.25
|
0.700 |
1.000 |
5 |
2014 |
2019 |
rs6687758
|
|
10
|
0.763 |
0.200 |
1 |
221991606 |
regulatory region variant
|
A/G
|
snv |
|
0.20
|
0.700 |
1.000 |
5 |
2010 |
2019 |
rs7229639
|
|
9
|
0.763 |
0.080 |
18 |
48924606 |
intron variant
|
A/G
|
snv |
|
0.87
|
0.700 |
1.000 |
5 |
2014 |
2019 |
rs10505477
|
|
11
|
0.658 |
0.400 |
8 |
127395198 |
intron variant
|
A/G
|
snv |
|
0.40
|
0.700 |
1.000 |
4 |
2007 |
2018 |
rs10774214
|
|
9
|
0.790 |
0.080 |
12 |
4259186 |
intron variant
|
T/C
|
snv |
|
0.54
|
0.700 |
1.000 |
4 |
2013 |
2019 |
rs10795668
|
|
9
|
0.724 |
0.160 |
10 |
8659256 |
upstream gene variant
|
G/A
|
snv |
|
0.24
|
0.700 |
1.000 |
4 |
2008 |
2019 |
rs11196172
|
|
9
|
0.708 |
0.200 |
10 |
112967084 |
intron variant
|
G/A
|
snv |
|
0.13
|
0.700 |
1.000 |
4 |
2014 |
2019 |
rs174537
|
|
14
|
0.708 |
0.400 |
11 |
61785208 |
non coding transcript exon variant
|
G/T
|
snv |
|
0.28
|
0.700 |
1.000 |
4 |
2014 |
2019 |
rs2423279
|
|
9
|
0.790 |
0.080 |
20 |
7831703 |
downstream gene variant
|
T/C
|
snv |
|
0.29
|
0.700 |
1.000 |
4 |
2013 |
2019 |
rs3184504
|
|
61
|
0.572 |
0.600 |
12 |
111446804 |
missense variant
|
T/A;C;G
|
snv |
0.67
|
|
0.700 |
1.000 |
4 |
2015 |
2019 |
rs3217810
|
|
10
|
0.776 |
0.080 |
12 |
4279105 |
intron variant
|
C/T
|
snv |
|
8.7E-02
|
0.700 |
1.000 |
4 |
2013 |
2019 |
rs3824999
|
|
9
|
0.790 |
0.080 |
11 |
74634505 |
intron variant
|
T/G
|
snv |
|
0.40
|
0.700 |
1.000 |
4 |
2012 |
2019 |
rs4779584
|
|
9
|
0.732 |
0.160 |
15 |
32702555 |
intergenic variant
|
T/C
|
snv |
|
0.67
|
0.700 |
1.000 |
4 |
2008 |
2015 |
rs6066825
|
|
10
|
0.776 |
0.080 |
20 |
48723580 |
intron variant
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
4 |
2015 |
2019 |
rs647161
|
|
9
|
0.776 |
0.080 |
5 |
135163402 |
intron variant
|
C/A
|
snv |
|
0.63
|
0.700 |
1.000 |
4 |
2013 |
2019 |
rs961253
|
|
9
|
0.732 |
0.240 |
20 |
6423634 |
intergenic variant
|
C/A
|
snv |
|
0.34
|
0.700 |
1.000 |
4 |
2008 |
2019 |
rs10411210
|
|
9
|
0.742 |
0.160 |
19 |
33041394 |
intron variant
|
C/T
|
snv |
|
0.22
|
0.700 |
1.000 |
3 |
2008 |
2019 |
rs1078643
|
|
10
|
0.776 |
0.080 |
17 |
10803924 |
missense variant
|
G/A;C
|
snv |
|
|
0.700 |
1.000 |
3 |
2019 |
2019 |
rs11190164
|
|
10
|
0.776 |
0.080 |
10 |
99591947 |
intergenic variant
|
A/G
|
snv |
|
0.19
|
0.700 |
1.000 |
3 |
2015 |
2019 |
rs12241008
|
|
9
|
0.716 |
0.160 |
10 |
112520943 |
intron variant
|
T/C
|
snv |
|
0.13
|
0.700 |
1.000 |
3 |
2014 |
2019 |