rs1050274678
|
|
3
|
0.925 |
0.040 |
21 |
45530803 |
missense variant
|
C/T
|
snv |
1.1E-05
|
7.0E-06
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs10824095
|
|
2
|
0.925 |
0.040 |
10 |
74176853 |
5 prime UTR variant
|
C/G;T
|
snv |
0.67
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs11719165
|
|
2
|
0.925 |
0.040 |
3 |
194865359 |
intergenic variant
|
T/C
|
snv |
|
0.53
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs12046844
|
|
2
|
0.925 |
0.040 |
1 |
65772696 |
regulatory region variant
|
G/A
|
snv |
|
0.17
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs1260186456
|
|
2
|
0.925 |
0.040 |
16 |
16102659 |
missense variant
|
G/T
|
snv |
9.4E-06
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs12720066
|
|
2
|
0.925 |
0.040 |
7 |
87540386 |
intron variant
|
A/C
|
snv |
|
3.9E-02
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs12934241
|
|
2
|
0.925 |
0.040 |
16 |
55486666 |
non coding transcript exon variant
|
C/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs1326123837
|
|
2
|
0.925 |
0.040 |
11 |
119025310 |
missense variant
|
C/T
|
snv |
|
7.0E-06
|
0.010 |
1.000 |
1 |
2020 |
2020 |
rs1422359334
|
|
2
|
0.925 |
0.040 |
7 |
143264131 |
missense variant
|
C/A;T
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs1424665740
|
|
2
|
0.925 |
0.040 |
13 |
103066068 |
missense variant
|
T/C
|
snv |
4.0E-06
|
7.0E-06
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs1453542
|
|
3
|
0.925 |
0.040 |
11 |
59457412 |
missense variant
|
G/A;C
|
snv |
7.2E-05;
0.26
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs1482105290
|
|
2
|
0.925 |
0.040 |
13 |
50012772 |
missense variant
|
A/G
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs149104283
|
|
4
|
0.882 |
0.040 |
12 |
20930928 |
intron variant
|
C/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1610696
|
|
2
|
0.925 |
0.040 |
6 |
29831026 |
3 prime UTR variant
|
C/G
|
snv |
|
0.29
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs17376848
|
|
3
|
0.925 |
0.040 |
1 |
97450068 |
synonymous variant
|
A/G
|
snv |
5.1E-02
|
4.3E-02
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs17501331
|
|
2
|
0.925 |
0.040 |
16 |
15995584 |
intron variant
|
A/G
|
snv |
|
7.7E-02
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs1885301
|
|
2
|
0.925 |
0.040 |
10 |
99781296 |
upstream gene variant
|
A/G
|
snv |
|
0.58
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1901440
|
|
2
|
0.925 |
0.040 |
2 |
133680388 |
intergenic variant
|
C/A
|
snv |
|
0.58
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs2074549
|
|
2
|
0.925 |
0.040 |
9 |
35061506 |
intron variant
|
T/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs3087403
|
|
2
|
0.925 |
0.040 |
2 |
99442408 |
missense variant
|
C/T
|
snv |
0.28
|
0.28
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs3136228
|
|
2
|
0.925 |
0.040 |
2 |
47782677 |
intron variant
|
T/G
|
snv |
|
0.30
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs3758581
|
|
3
|
0.925 |
0.040 |
10 |
94842866 |
missense variant
|
A/G
|
snv |
|
0.95
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs3825876
|
|
2
|
0.925 |
0.040 |
15 |
84892637 |
intron variant
|
G/A
|
snv |
|
0.34
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs4148396
|
|
2
|
0.925 |
0.040 |
10 |
99832187 |
intron variant
|
T/C
|
snv |
|
0.65
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs4150558
|
|
3
|
0.882 |
0.040 |
11 |
18332808 |
non coding transcript exon variant
|
T/A
|
snv |
|
8.7E-03
|
0.010 |
1.000 |
1 |
2017 |
2017 |