rs7953249
|
|
4
|
0.882 |
0.160 |
12 |
120965921 |
splice region variant
|
G/A
|
snv |
|
0.59
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs8037137
|
|
8
|
0.807 |
0.160 |
15 |
90963407 |
upstream gene variant
|
T/C
|
snv |
|
0.19
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs8098244
|
|
2
|
0.925 |
0.120 |
18 |
23825589 |
intron variant
|
A/C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs9870207
|
|
1
|
1.000 |
0.040 |
3 |
190807727 |
intergenic variant
|
A/G
|
snv |
|
0.43
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs1011970
|
|
22
|
0.677 |
0.320 |
9 |
22062135 |
intron variant
|
G/T
|
snv |
|
0.23
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1057941
|
|
18
|
0.701 |
0.280 |
1 |
155216951 |
non coding transcript exon variant
|
G/A;T
|
snv |
0.46
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs11119608
|
|
17
|
0.708 |
0.280 |
1 |
210816167 |
intron variant
|
T/G
|
snv |
|
0.21
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs11168936
|
|
17
|
0.708 |
0.280 |
12 |
49251457 |
intron variant
|
T/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs11200014
|
|
19
|
0.695 |
0.280 |
10 |
121575416 |
intron variant
|
G/A;T
|
snv |
|
0.34
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs115392158
|
|
17
|
0.708 |
0.280 |
6 |
31347004 |
intron variant
|
A/G
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs115707823
|
|
19
|
0.701 |
0.320 |
6 |
30374976 |
intergenic variant
|
G/A
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs11571818
|
|
17
|
0.708 |
0.280 |
13 |
32394673 |
intron variant
|
T/C
|
snv |
6.6E-03
|
6.0E-03
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs11571833
|
|
43
|
0.608 |
0.360 |
13 |
32398489 |
stop gained
|
A/T
|
snv |
6.6E-03
|
6.0E-03
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs11844632
|
|
17
|
0.708 |
0.280 |
14 |
68559662 |
intron variant
|
G/A
|
snv |
|
0.23
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs11907546
|
|
17
|
0.708 |
0.280 |
20 |
34131991 |
upstream gene variant
|
C/A;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs12601991
|
|
17
|
0.708 |
0.280 |
17 |
37741642 |
intron variant
|
T/A;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs141752671
|
|
17
|
0.708 |
0.280 |
11 |
103745837 |
intron variant
|
A/G
|
snv |
|
5.4E-03
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs147527678
|
|
17
|
0.708 |
0.280 |
6 |
32699696 |
intergenic variant
|
G/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs147680653
|
|
17
|
0.708 |
0.280 |
6 |
29785031 |
intergenic variant
|
A/G
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs148883465
|
|
17
|
0.708 |
0.280 |
11 |
103813371 |
intron variant
|
A/G
|
snv |
|
7.2E-03
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1862626
|
|
17
|
0.708 |
0.280 |
5 |
56737113 |
regulatory region variant
|
G/T
|
snv |
|
0.68
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs186507655
|
|
17
|
0.708 |
0.280 |
1 |
1351675 |
upstream gene variant
|
G/A
|
snv |
|
6.8E-03
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs2300206
|
|
17
|
0.708 |
0.280 |
20 |
34002002 |
intron variant
|
G/C;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs2974935
|
|
17
|
0.708 |
0.280 |
1 |
155212052 |
non coding transcript exon variant
|
G/A;C;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs3184504
|
|
92
|
0.572 |
0.600 |
12 |
111446804 |
missense variant
|
T/A;C;G
|
snv |
0.67
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |