rs6983267
|
|
62
|
0.578 |
0.440 |
8 |
127401060 |
non coding transcript exon variant
|
G/T
|
snv |
|
0.37
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs121434569
|
|
70
|
0.581 |
0.520 |
7 |
55181378 |
missense variant
|
C/T
|
snv |
2.8E-05
|
5.6E-05
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs2231142
|
|
56
|
0.583 |
0.680 |
4 |
88131171 |
missense variant
|
G/C;T
|
snv |
4.0E-06;
0.12
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs20541
|
|
52
|
0.585 |
0.720 |
5 |
132660272 |
missense variant
|
A/G
|
snv |
0.72
|
0.77
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1051740
|
|
56
|
0.592 |
0.760 |
1 |
225831932 |
missense variant
|
T/C
|
snv |
0.32
|
0.27
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs17655
|
|
52
|
0.597 |
0.560 |
13 |
102875652 |
missense variant
|
G/C
|
snv |
0.28
|
0.30
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs351855
|
|
58
|
0.597 |
0.560 |
5 |
177093242 |
missense variant
|
G/A
|
snv |
0.33
|
0.26
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs243865
|
|
48
|
0.600 |
0.640 |
16 |
55477894 |
intron variant
|
C/T
|
snv |
|
0.19
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs1205
|
|
46
|
0.602 |
0.680 |
1 |
159712443 |
3 prime UTR variant
|
C/T
|
snv |
|
0.30
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs2070744
|
|
54
|
0.608 |
0.680 |
7 |
150992991 |
intron variant
|
C/T
|
snv |
|
0.70
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs895819
|
|
46
|
0.623 |
0.560 |
19 |
13836478 |
non coding transcript exon variant
|
T/A;C;G
|
snv |
0.34
|
0.38
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs10889677
|
|
40
|
0.627 |
0.720 |
1 |
67259437 |
3 prime UTR variant
|
C/A
|
snv |
|
0.27
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs920778
|
|
36
|
0.633 |
0.480 |
12 |
53966448 |
intron variant
|
G/A
|
snv |
|
0.57
|
0.030 |
1.000 |
3 |
2017 |
2019 |
rs727503094
|
|
41
|
0.633 |
0.440 |
11 |
534287 |
missense variant
|
GC/AG;AT;TA;TT
|
mnv |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs121913364
|
|
34
|
0.641 |
0.520 |
7 |
140753334 |
missense variant
|
T/C;G
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs4759314
|
|
31
|
0.649 |
0.440 |
12 |
53968051 |
non coding transcript exon variant
|
G/A
|
snv |
|
0.93
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs121913227
|
|
31
|
0.653 |
0.320 |
7 |
140753336 |
missense variant
|
AC/CT;TT
|
mnv |
|
|
0.020 |
1.000 |
2 |
2005 |
2019 |
rs763110
|
|
30
|
0.653 |
0.560 |
1 |
172658358 |
upstream gene variant
|
C/T
|
snv |
|
0.49
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs10505477
|
|
31
|
0.658 |
0.400 |
8 |
127395198 |
intron variant
|
A/G
|
snv |
|
0.40
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs145204276
|
|
31
|
0.658 |
0.320 |
1 |
173868254 |
splice donor variant
|
CAAGG/-
|
delins |
|
8.8E-02
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1800624
|
|
33
|
0.658 |
0.480 |
6 |
32184610 |
upstream gene variant
|
A/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs74799832
|
|
33
|
0.662 |
0.280 |
10 |
43121968 |
missense variant
|
T/C
|
snv |
4.0E-06
|
|
0.020 |
1.000 |
2 |
2012 |
2017 |
rs2839698
|
|
25
|
0.662 |
0.520 |
11 |
1997623 |
non coding transcript exon variant
|
G/A
|
snv |
0.41
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs2071559
|
|
26
|
0.667 |
0.680 |
4 |
55126199 |
upstream gene variant
|
A/G
|
snv |
|
0.53
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs531564
|
|
27
|
0.672 |
0.480 |
8 |
9903189 |
non coding transcript exon variant
|
G/C
|
snv |
|
0.14
|
0.020 |
0.500 |
2 |
2015 |
2018 |