rs1279653488
|
|
1
|
1.000 |
0.040 |
17 |
64047898 |
missense variant
|
G/A
|
snv |
|
7.0E-06
|
0.700 |
|
0 |
|
|
rs11200014
|
|
19
|
0.695 |
0.280 |
10 |
121575416 |
intron variant
|
G/A;T
|
snv |
|
0.34
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs56084662
|
|
18
|
0.701 |
0.280 |
13 |
32295727 |
3 prime UTR variant
|
G/A
|
snv |
|
3.5E-03
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs56404467
|
|
17
|
0.708 |
0.280 |
13 |
32265853 |
intron variant
|
G/A
|
snv |
|
1.3E-02
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs116046250
|
|
1
|
1.000 |
0.040 |
15 |
26986803 |
intron variant
|
T/G
|
snv |
|
1.5E-02
|
0.700 |
1.000 |
1 |
2019 |
2019 |
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 |
rs6755777
|
|
3
|
0.882 |
0.120 |
2 |
176178498 |
non coding transcript exon variant
|
T/A;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs115392158
|
|
17
|
0.708 |
0.280 |
6 |
31347004 |
intron variant
|
A/G
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs7953249
|
|
4
|
0.882 |
0.160 |
12 |
120965921 |
splice region variant
|
G/A
|
snv |
|
0.59
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs11651755
|
|
9
|
0.763 |
0.160 |
17 |
37739849 |
intron variant
|
T/C
|
snv |
|
0.52
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs12601991
|
|
17
|
0.708 |
0.280 |
17 |
37741642 |
intron variant
|
T/A;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs7405776
|
|
6
|
0.807 |
0.120 |
17 |
37733029 |
intron variant
|
G/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs711830
|
|
3
|
0.882 |
0.120 |
2 |
176172583 |
3 prime UTR variant
|
A/C;G;T
|
snv |
|
0.76
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs11119608
|
|
17
|
0.708 |
0.280 |
1 |
210816167 |
intron variant
|
T/G
|
snv |
|
0.21
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs73110464
|
|
17
|
0.708 |
0.280 |
12 |
52918828 |
intron variant
|
C/T
|
snv |
|
0.12
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs8098244
|
|
2
|
0.925 |
0.120 |
18 |
23825589 |
intron variant
|
A/C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs1400482
|
|
2
|
0.925 |
0.120 |
8 |
128529685 |
intron variant
|
G/A
|
snv |
|
0.13
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs150293538
|
|
1
|
1.000 |
0.040 |
8 |
76408119 |
intron variant
|
C/T
|
snv |
|
1.4E-02
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs79079890
|
|
1
|
1.000 |
0.040 |
10 |
3641956 |
intergenic variant
|
T/G
|
snv |
|
0.10
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs192876988
|
|
4
|
0.851 |
0.120 |
4 |
79376097 |
intergenic variant
|
T/C
|
snv |
|
1.6E-02
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs75316749
|
|
18
|
0.701 |
0.280 |
3 |
169043635 |
intergenic variant
|
A/G
|
snv |
|
4.2E-02
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1411105125
|
|
1
|
1.000 |
0.040 |
19 |
12873875 |
missense variant
|
C/T
|
snv |
|
|
0.700 |
|
0 |
|
|
rs144962376
|
|
2
|
0.925 |
0.120 |
10 |
21589903 |
intron variant
|
CCCCTT/-;CCCCTTCCCCTT
|
delins |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
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 |
rs481519
|
|
17
|
0.708 |
0.280 |
3 |
27285723 |
intron variant
|
C/A;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |