rs8044769
|
|
6
|
0.851 |
0.200 |
16 |
53805223 |
intron variant
|
T/A;C;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs833058
|
|
3
|
0.925 |
0.120 |
6 |
43764117 |
regulatory region variant
|
C/T
|
snv |
|
0.53
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs6976
|
|
4
|
0.851 |
0.080 |
3 |
52694788 |
3 prime UTR variant
|
C/T
|
snv |
0.38
|
0.33
|
0.710 |
1.000 |
3 |
2015 |
2019 |
rs9350591
|
|
2
|
0.925 |
0.040 |
6 |
75531811 |
intergenic variant
|
C/A;T
|
snv |
|
0.12
|
0.710 |
1.000 |
3 |
2015 |
2019 |
rs11730582
|
|
10
|
0.807 |
0.240 |
4 |
87975269 |
non coding transcript exon variant
|
T/C
|
snv |
|
0.37
|
0.010 |
< 0.001 |
1 |
2015 |
2015 |
rs17524488
|
|
4
|
0.925 |
0.040 |
4 |
87975555 |
non coding transcript exon variant
|
-/G
|
delins |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs3117582
|
|
14
|
0.716 |
0.440 |
6 |
31652743 |
intron variant
|
T/G
|
snv |
|
7.1E-02
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs5009270
|
|
1
|
1.000 |
0.040 |
7 |
112519123 |
upstream gene variant
|
G/A;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs835487
|
|
2
|
0.925 |
0.040 |
12 |
104666989 |
intron variant
|
A/G
|
snv |
|
0.43
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs835488
|
|
1
|
1.000 |
0.040 |
12 |
104667230 |
intron variant
|
C/T
|
snv |
|
0.41
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs2707466
|
|
2
|
1.000 |
0.040 |
7 |
121339035 |
missense variant
|
C/G;T
|
snv |
0.44
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs754106
|
|
1
|
1.000 |
0.040 |
13 |
46578520 |
intron variant
|
C/T
|
snv |
|
0.63
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs10492367
|
|
3
|
0.882 |
0.040 |
12 |
27862037 |
regulatory region variant
|
G/T
|
snv |
|
0.12
|
0.700 |
1.000 |
2 |
2018 |
2019 |
rs10843013
|
|
1
|
1.000 |
0.040 |
12 |
27872263 |
intergenic variant
|
A/C
|
snv |
|
0.15
|
0.700 |
1.000 |
2 |
2018 |
2018 |
rs10896015
|
|
1
|
1.000 |
0.040 |
11 |
65556254 |
intron variant
|
G/A
|
snv |
|
0.26
|
0.700 |
1.000 |
2 |
2018 |
2019 |
rs10948172
|
|
3
|
0.882 |
0.040 |
6 |
44809954 |
intron variant
|
A/G
|
snv |
|
0.27
|
0.700 |
1.000 |
2 |
2018 |
2019 |
rs12209223
|
|
2
|
1.000 |
0.040 |
6 |
75454873 |
intron variant
|
C/A
|
snv |
|
7.3E-02
|
0.700 |
1.000 |
2 |
2018 |
2019 |
rs12901372
|
|
1
|
1.000 |
0.040 |
15 |
67078168 |
intron variant
|
C/A;G
|
snv |
|
|
0.700 |
1.000 |
2 |
2018 |
2019 |
rs2521349
|
|
2
|
0.925 |
0.040 |
17 |
69507360 |
intron variant
|
G/A;T
|
snv |
|
|
0.700 |
1.000 |
2 |
2018 |
2018 |
rs2785988
|
|
2
|
0.925 |
0.040 |
1 |
219570796 |
intergenic variant
|
C/A
|
snv |
|
0.23
|
0.700 |
1.000 |
2 |
2018 |
2019 |
rs2820436
|
|
4
|
0.882 |
0.040 |
1 |
219467338 |
intergenic variant
|
A/C;G
|
snv |
|
|
0.700 |
1.000 |
2 |
2018 |
2018 |
rs4252548
|
|
4
|
1.000 |
0.040 |
19 |
55368304 |
missense variant
|
C/T
|
snv |
2.1E-02
|
1.8E-02
|
0.710 |
1.000 |
2 |
2018 |
2019 |
rs4836732
|
|
2
|
1.000 |
0.040 |
9 |
116504416 |
intron variant
|
C/T
|
snv |
|
0.49
|
0.700 |
1.000 |
2 |
2018 |
2019 |
rs7222178
|
|
1
|
1.000 |
0.040 |
17 |
61574921 |
TF binding site variant
|
T/A
|
snv |
|
0.26
|
0.700 |
1.000 |
2 |
2018 |
2019 |
rs763780
|
|
87
|
0.531 |
0.720 |
6 |
52236941 |
missense variant
|
T/C
|
snv |
6.7E-02
|
6.6E-02
|
0.020 |
1.000 |
2 |
2018 |
2019 |