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 |
rs10962692
|
|
3
|
0.925 |
0.120 |
9 |
16915876 |
upstream gene variant
|
G/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs11168936
|
|
17
|
0.708 |
0.280 |
12 |
49251457 |
intron variant
|
T/A;C
|
snv |
|
|
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 |
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 |
rs144962376
|
|
2
|
0.925 |
0.120 |
10 |
21589903 |
intron variant
|
CCCCTT/-;CCCCTTCCCCTT
|
delins |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
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 |
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 |
rs481519
|
|
17
|
0.708 |
0.280 |
3 |
27285723 |
intron variant
|
C/A;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs62274041
|
|
3
|
0.925 |
0.120 |
3 |
156717851 |
upstream gene variant
|
G/A;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs6755777
|
|
3
|
0.882 |
0.120 |
2 |
176178498 |
non coding transcript exon variant
|
T/A;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs7405776
|
|
6
|
0.807 |
0.120 |
17 |
37733029 |
intron variant
|
G/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs7705526
|
|
15
|
0.776 |
0.240 |
5 |
1285859 |
intron variant
|
C/A;T
|
snv |
|
|
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 |
rs1411105125
|
|
1
|
1.000 |
0.040 |
19 |
12873875 |
missense variant
|
C/T
|
snv |
|
|
0.700 |
|
0 |
|
|
rs1490428165
|
|
1
|
1.000 |
0.040 |
9 |
27209192 |
missense variant
|
C/G;T
|
snv |
4.0E-06
|
|
0.700 |
|
0 |
|
|
rs199897804
|
|
1
|
1.000 |
0.040 |
X |
18604645 |
missense variant
|
C/A;T
|
snv |
4.9E-05
|
|
0.700 |
|
0 |
|
|
rs746442213
|
|
1
|
1.000 |
0.040 |
2 |
29232307 |
missense variant
|
C/A;T
|
snv |
4.0E-06;
1.2E-05
|
|
0.700 |
|
0 |
|
|
rs1279653488
|
|
1
|
1.000 |
0.040 |
17 |
64047898 |
missense variant
|
G/A
|
snv |
|
7.0E-06
|
0.700 |
|
0 |
|
|
rs540521894
|
|
1
|
1.000 |
0.040 |
1 |
156864760 |
missense variant
|
C/A;T
|
snv |
4.0E-06;
5.6E-05
|
2.1E-05
|
0.700 |
|
0 |
|
|